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US3779241A - Intrauterine contraceptive device and method for its use - Google Patents

Intrauterine contraceptive device and method for its use
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US3779241A
US3779241AUS00190780AUS3779241DAUS3779241AUS 3779241 AUS3779241 AUS 3779241AUS 00190780 AUS00190780 AUS 00190780AUS 3779241D AUS3779241D AUS 3779241DAUS 3779241 AUS3779241 AUS 3779241A
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hollow body
walls
uterine cavity
intrauterine contraceptive
contraceptive device
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W Vennard
J Wright
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Ethyl Corp
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Ethyl Corp
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Abstract

A method and apparatus for birth control utilizing an intrauterine contraceptive device which includes a preformed, hollow body with thin, flexible walls, the hollow body having the approximate size and shape of the uterine cavity. A flexible, compressible, filler material substantially completely fills the hollow body so that the walls of the hollow body make contact with a major portion of the walls of the uterine cavity when the device is in position within the uterine cavity. In a preferred form, the hollow body is filled with a polymerizable organosiloxane material after being placed in the uterine cavity and the material is then polymerized to produce a device having substantially the size and shape of a normal uterine cavity.

Description

United States Patent [1 1 Vennard et a1.
l l Dec. 18, 1973 [75] Inventors: William O. Vennard; Jack C.
Wright, both of Baton Rouge, La.
[73] Assignee: Ethyl Corporation, New York, NY.
[22] Filed: Oct. 20, 1971 [21] Appl, No.: 190,780
[52] US. Cl. 128/129 [51} Int. Cl. A6 5/46 [58] Field of Search 128/127, 128, 129,
[56] References Cited UNITED STATES PATENTS 3,306,286 2/1967 Ahmed 128/130 Primary Examiner-Richard A. Gaudet Assistant Examiner-G. F. Dunne At!0rm' vDonald L. Johnson et al.
[5 7 1 ABSTRACT A method and apparatus for birth control utilizing an intrauterine contraceptive device which includes a preformed, hollow body with thin, flexible walls, the hollow body having the approximate size and shape of the uterine cavity. A flexible, compressible, filler material substantially completely fills the hollow body so that the walls of the hollow body make Contact with a major portion of the walls of the uterine cavity when the device is in position within the uterine cavity. In a preferred form, the hollow body is filled with a polymerizable organosiloxane material after being placed in the uterine cavity and the material is then polymerized to produce a device having substantially the size and shape of a normal uterine cavity.
11 Claims, 12 Drawing Figures Pmmennzmms 3779.241SHEET 18F 2 FIG 3. FIG. 4.
Pmmmnu: 1 a mu 3779.241 sum 2 w 2 3| 26 FIG. 6A. FIG. 7A.
FIG. 5B.
INTRAU'IERINE CONTRACEPTIVE DEVICE AND METHOD FOR ITS USE BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates, in general, to a method and apparatus for birth control utilizing a novel intrauterine contraceptive device.
2. Description of the Prior Art Intrauterine contraceptive devices are well known in the art and have been in wide use for many years. The devices are fabricated from many different materials and take the form of spirals, loops, bows, rings, etc., as exemplified by devices known asthe Lippes loop, Margulies spiral, Birnberg bow and the Grafenberg ring. Very early devices were made from silver metal; however, their use has declined and thermoplastic material has replaced the former metal structures.
Many of the prior art intrauterine contraceptive devices suffer from two principal deficiencies which have prevented their widespread adoption by the medical profession. In very early work with intrauterine contraceptive devices, it was discovered that the natural contractions of the uterine cavity would expel the earlier devices from the uterus and lead to unwanted pregnancies when the female was unaware that the device had been expelled. This lead to designing the intrauterine devices into very elaborate configurations in order to permit compression and collapse for insertion through the cervix into the uterus and subsequent expansion in the uterus to assume a form which would not be easily expelled by the natural muscle contractions. The second problem associated with the prior art intrauterine contraceptive devices has been the tendency of these devices to produce physiological complications in the patient. Many women are unable to accommodate intrauterine contractptive devices because of inflammation and irritation and sometimes bleeding which occurs in certain patients.
A recent study of IUDs by E. J. David, M.D., and John Lesinski, M.D., has been published inVolume 36, No. 3, September 1970 issue of Obstetrics and Gynecology entitled Mechanism of Action of Intrauterine Contraceptives in Women." The conclusion is reached in this article that the contraceptive efficacy of devices molded of plastic materials of similar composition correlates with the total surface area of the plastic article coming in contact with the endometrium, irrespective of the variations in geometric design. Further, the authors observed that chemical composition of the device significantly influences pregnancy rates when the rates accompanying devices of identical size, shape and surface area are compared. In the studies conducted, it was found that an IUD constructed in the form of a shield had the lowest percent pregnancy rate of any of the comparative devices tested, e.g., a B loop and a double coil. Efficiency for this shield-shaped IUD was' 98.9 percent pregnancy prevention. While the device disclosed in the foregoing study is an improvement over prior art IUDs, nevertheless, there exists the problem of placing the device within the uterus. Because of its size and configuration, it is difficult to collapse the device into a sufficiently small size to permit convenient insertion through the dilated cervical canal. Further, after entry, opening the device and positioning it properly between the walls of the uterus presents significant problems.
Therefore, there is a need in the IUD art to provide a device which can contact as much of the uterine wall area as possible and yet permit easy placement within the uterus and easy withdrawal therefrom, if it is desired to remove the device.
SUMMARY OF THE INVENTION It is an object of the present invention to provide an intrauterine contraceptive device which provides maxi mum surface area contact between the walls of the device and the walls of the uterus.
It is a further object of the present invention to provide an intrauterine contraceptive device which may be readily placed in the uterus and also readily removed therefrom.
It is also an object of the present invention to provide an intrauterine contraceptive device which has a shape substantially the same as that of the uterine cavity.
It is still another object of the present invention to provide an intrauterine contraceptive device which is flexible and compressible so as not to produce significant irritation of the walls of the uterus.
The foregoing objects are realized in an intrauterine contraceptive device which includes a preformed hollow body having thin, flexible walls which have the approximate size and shape of the uterine cavity. A flexible, compressible, filler material substantially completely fills the hollow body, whereby the walls of the hollow body will make contact with a major portion of the walls of the uterine cavity when the device is positioned in the uterine cavity.
The method aspects of the present invention are realized in a method of birth control comprising the steps of positioning a preformed, hollow body having thin, flexible walls within the uterine cavity and expanding said body to substantially fill the cavity.
The intrauterine contraceptive device of the present invention overcomes the disadvantage found in prior art devices by providing maximum contact between the IUD and the walls of the uterus. The IUD of the present invention also overcomes the difficulty of fitting IUD's to various women having uteri of significantly different sizes. By preparing the IUD of the present invention in the form of a flexible, thin wall, hollow body shaped like the uterus, the device, when placed in the uterus and filled, is made to substantially fit the contours of the uterus and substantially fill the same. By forming the hollow body portion of the IUD of the present invention out of thin wall, flexible, soft, collapsible, polymeric material, e.g., natural rubber or silicone rubber, and hollow body can be folded or collapsed for easy in sertion into the uterus through the cervical passage. By utilizing either a removable filler material, such as air or water, or a solid filler material which is easily compressed, such as a foamed elastomeric material, the
IUD of the present invention can be easily withdrawn from the uterus.
BRIEF DESCRIPTION OF THE DRAWING FIG. 1 is a side, elevational, sectional view of the human female reproductive organs showing one embodiment of the IUD of the present invention in place in the uterus;
FIG. 2 is a plan, sectional, partially broken view of FIG. 1 taken along theline 22;
FIG. 4 is a perspective, elevational, partially broken view of still another embodiment of the IUD of the present invention;
FIG. 4A is a cross-sectional view of FIG. 4 taken along line 4A4A;
' FIG. 5 is a plan view of a further embodiment of the IUD of the present invention;
FIG. 5A is a cross-sectional view of FIG. 5 taken alongline 5A-5A;
FIG. 5B is a cross-sectional view of FIG. 5 taken along line 58-58;
FIG. 6 is a plan view of a still further embodiment of the IUD of the present invention;
FIG. 6A is a cross-sectional view of FIG. 6 taken along line 6A6A;
FIG. 7 is a plan view ofa different embodiment of the IUD of the present invention; and
FIG. 7A is a cross-sectional view of FIG. 7 taken along line 7A7A.
DESCRIPTION OF THE PREFERRED EMBODIMENTS contact with the walls 11b of the uterus. The hollow body includes a thin, flexibletop wall 19 and abottom wall 20. When inflated, the hollow body generally has the shape of an equilateral triangle having generally parabolic sides. The hollow body includes two spaced apart, substantially equal length, left andright leg portions 12 and 13 which project into the horns or the respective left and right Fallopian tube entrances l4 and 15. Thelower neck portion 16 of the hollow body is elongated and is received in thecervical canal 17. The lower end of the neck portion terminates in the cervical canal just short of its entrance into thevagina 18. Aplug 21 made of soft elastomeric material, which may be integrally formed on the end ofneck 16, closes the open end ofneck portion 16 and permits the collapsed, hollow body to be inflated by means of a hypodermic needle and syringe.
Another embodiment of the IUD of the present invention is shown in FIG. 3. Thehollow body 10 in this embodiment is filled with aliquid material 22 in place of a gaseous medium used in the embodiment shown in FIGS. 1 and 2. The liquid filling material may be any suitable sterile liquid such as water, mineral oil, medical grade silicone fluids, saline solutions, or any other non-toxic sterile liquid.
In another embodiment of the invention, the fluids used to fill the hollow body have dissolved or suspended therein suitable. concentrations of bacteriostatic agents or medicants, and the hollow bodies are made of a liquid-permeable film so that a very gradual release of the fluid from the hollow body to the uterus occurs. 'Among suitable bacteriostatic materials are 2,- 2'-thiobis-(4,6-dichlorophenol) (sold under the trademark Actomer by Monsanto Chemical Company) and 2,2'-methylenebis(3,4,6-trichlorophenol) (sold under the trademark Hexachlorophcne" by Sindar Corporation). Suitable medicants are the penieillins.
and the sulfa drugs. Other bacteriostatic agents and medicants may also be used.
In a further embodiment of the present invention, the bacteriostatic agents or medicants may be incorporated into the film-forming material of the hollow bodies, e.g., by mixing with the plastic material prior to forming the hollow body (see U. S. Pat. No. 2,919,200) or by impregnating the hollow body after being formed.
A still further embodiment of the present invention is to incorporate natural and synthetic fragrances in the fluids contained within the liquid-permeable hollow body.
Still another embodiment of the IUD of the present invention is shown in FIGS. 4 and 4A. The preformedbody 10 is first collapsed or folded and inserted into the uterus. The body is then filled by means of a hypodermic syringe and needle with a liquid-curable or polymerizable material, such as a prepolymer or a monomer containing a curing agent or polymerization cata lyst. The material is then allowed to cure or polymerize to provide a solid or cellular, flexible, compressible filler insert having the exact shape of the uterus. As seen in FIG. 4A, thefiller insert 23 is formed ofa cellular material produced by adding any suitable foaming agent to the liquid material used to form the filler insert. Preferred are foaming agents which have boiling points slightly below the normal temperature of the human body, i.e., below 982 F, such as isopentane, n-butane, dimethyl ether, diethyl ether, ethyl chloride, 2,2'-azobis(2,4-dimethylvaleronitrile), and others.
Theupper wall 19 and thelower wall 20 of the hollow body may be joined by an integrally formed connector stem orrib 24 as seen more clearly in FIG. 4A. This stem or rib prevents excessive thickening of the IUD so that the entire IUD may be removed from the uterus through thecervical canal 17 when dilated. It has been observed that the muscle tone of the upper and lower wall sections of the uterus is weakened in women who have experienced multiple childbirth. This condition results in the filler material assuming an undesirable, semi-spherical, cross-sectional shape rather than the desired, elliptical, cross-sectional shape, as shown in FIG. 4A. The stem orrib 24 prevents undue thickening of the IUD in those uteri having poor muscle tone.
As seen in FIGS. I4A, the IUD of the present invention, when expanded with a filling material, will have its maximum thickness at the mid-portion thereof where the uterus has its normal maximum diameter. The depiction of the IUD of the present invention, as seen in FIGS. l-4A, represents an average of the shape that the device is expected to assume; however, it is understood that the final shape of the IUD of the present in vention will be determined solely by the shape of the individual uterus in which the device is placed, or in part by the length of thestem 24 when this form of the IUD is utilized.
In FIGS. 5, 5A and 5B, another embodiment of the IUD of the present invention is depicted. The hollow body, or envelope, 25 is formed from a thin wall, flexible material and has atop wall 26 and abottom wall 27. The top and bottom walls are welded together, as by being integrally formed, in a pluraity of spaced apart, generallyrectangular sections 28 which extend in wardly from the side edges 2929 of thebody 25. Top,
intermediate and bottom, hollow, transverse channels 30, 30a and 30b are provided inbody 25 between the fused top and bottom wall areas. These transverse channels intersect alongitudinal channel 31 which is an extension of the bore defined by thestem 32 of the hollow body. The stem is closed byplug 33.
Thehollow body 34, as seen in FIGS. 6 and 6A, has the same general shape as that ofhollow body 25, but is provided with a centrally locatedarea 39 which has the shape of an equilateral triangle wherein the top andbottom walls 35 and 36 are fused together. A triangularly shaped,hollow channel 37 surrounds the fusedarea 39 and joins the bore provided in stem 38.
In FIGS. 7 and 7A, another embodiment of thehollow body 40 is shown whereintop wall 41 andbottom wall 42 are joined together along spaced-apart, parallel lines 43-43 which extend inwardly from thetop edge 44 of the body.
In all of the embodiments shown in FIGS. 5-7A, the fused portions of the top and bottom walls limit transverse expansion of the hollow body when the hollow body is expanded in the uterus by filling with the selected filling material, e.g., water, air, silicone rubber. However, the constructions still provide for a substantial contact between the wall areas of the lUDs and the walls of the uterus which has been determined to be directly related to the efficiency of an IUD in preventing pregnancy. The top and bottom walls of the IUDs of the present invention may be joined by any suitable means at any number of points.
The hollow body portion of the IUD may be made from any suitable material which is non-toxic, flexible, and capable of forming a reasonably strong, thin film. Among suitable materials for forming the hollow body are silicone rubbers (organosiloxane polymers), synthetic rubbers, natural rubbers, polyethylene, polypropylene, plasticized polyvinyl chloride, plasticized polyvinylidene chloride, polyvinyl alcohol, polyesters, polyethers, polyvinyl acetate, polyethylene oxide, polyurethanes, polyvinyl pyrrolidone, and water soluble polystarches and polycellulosics.
The hollow body can be formed by fusing thin sheets of the material precut in the desired shape of the hollow body. A preferred method for forming the hollow body when using elastomeric type materials is by dipping a mold having the desired shape into a latex solution and curing the latex which adheres to the mold. Rotational molding using hollow molds of the desired shape can also be used. Resin monomers and prepolymers may also be used to form the hollow body by coating a mold having the shape of the walls of the uterus and then polymerizing the monomer or prepolymer.
When it is desired to use a solid or semi-solid filler material for the IUD, these filler materials may be formed in situ in the hollow body after placing the hollow body within the uterus by curing any curable material which produces a soft, elastomeric polymer. It is preferred that the filler material be formed of a nonirritating, flexible, elastomeric material, particularly one prepared from a polyorganosiloxane material. Among the preferred materials are the medical grade silicone rubber prepolymers marketed by Dow-Corning under the trade name Silastic. In certain applications, Dow-Coming medical adhesive Type A may be used as the prepolymer and catalyzed to provide the polymerized, finished IUD device. The preferred material for forming the filler material of the IUD of the present invention is Dow-Cornings Silastic RT-382 which is a room-temperature-curing silicone rubber or prepolymer. The viscosity of Silastic RT-382 can be reduced by mixing with Dow-Corning RTV thinner (dimethyl siliconefluid) to achieve the desired viscosity for injecting the prepolymer into the hollow body using a hypodermic syringe.
In the method of the present invention, the deflatedhollow body 10 is rolled into a tubular conformation or otherwise folded into a compact tubular shape. It is then placed in a hollow insertion device for insertion into the uterus through the vagina and cervical canal. U. S. Pat. No. 3,509,877 discloses a suitable insertion device and its disclosure is hereby incorporated by reference. After placement in the uterus, thehollow body 10 is inflated by piercingplug 18 with a hypodermic needle and forcing the selected filler material through the needle from a filled hypodermic syringe. To remove the device when it is filled with a gas or a liquid, the operation described above is reversed to empty the hollow body and permit its collapse for easy withdrawal. Theneck 16 can then be grasped with a suitable instrument and the device removed through the cervix, which may be dilated if necessary. When a solid or semi-solid filler is used, it is recommended that the cervix be dilated before removing the IUD.
Another embodiment of the IUD of the present invention is prepared using water soluble polymers such as polyvinyl pyrrolidone (PVP), polystarches, polycellulosics, and polyvinyl alcohol (PVA) to fabricate the hollow body. These materials are soluble in the uterine fluids and a hollow body made from these polymers, when placed in the uterus and filled with a filler that polymerizes in situ, e.g., silicone prepolymer, will dissolve and leave the polymerized silicone material in the uterus to serve as the IUD.
From the foregoing examples of exemplary embodiments of the invention, it is seen that numerous modifications and changes will readily occur to those skilled in the art. Thus, the exact construction and operation described hereinbefore is not to be taken to limit the invention, and all embodiments coming within the scope of the claims are intended to be covered herein.
What is claimed is:
1. An intrauterine contraceptive device comprising: a preformed hollow body having a shape approximating an equilateral triangle with a continuous, imperforate top wall joined at its periphery to a continuous, imperforate bottom wall, said walls being formed of a thin, flexible material and being connected to each other by connector stem means at one or more points intermediate their peripheries to limit expansion of said body; means defining an opening in one of the apices of said hollow body for filling and emptying said hollow body;
means closing said opening; and a flexible, compressible, filler material substantially completely filling said hollow body whereby the walls of said body will make contact with a major portion of the walls of said uterine cavity when said device is positioned in said uterine cavity.
2. The intrauterine contraceptive device of claim 1 wherein said hollow body is made from a material selected from the group consisting of organosiloxane polymers, synthetic rubber, natural rubber, polyethylene, polypropylene, plasticized polyvinyl chloride, plasticized polyvinylidene chloride, polyvinyl alcohol, polyesters, polyethers, polvinyl acetate, polyethylene oxide, polyurethanes, polyvinyl pyrrolidone, and water soluble polystarches and polycellulosics.
3. The intrauterine contraceptive device of claim 1 wherein said hollow body has fixedly attached thereto means for engaging said hollow body for removing said hollow body from the uterine cavity.
4. The intrauterine contraceptive device of claim 1 wherein said means for engaging said body includes a thin, hollow, elongated stem.
5. The intrauterine contraceptive device of claim 4 wherein said stem is closed by a flexible plug.
6. The intrauterine countraceptive device of claim 1 wherein said top and bottom walls are connected together substantially at their center by a single said connector stern means which is integrally formed with said top and bottom walls.
7. The intrauterine contraceptive device of claim 1 wherein said hollow body is made from a material which is soluble in the fluids normally present in the uterine cavity and said hollow body serves as a mold for a permanent intrauterine contraceptive device produced by filling said hollow body with a fluid polymerizable prepolymer or monomer after said hollow body is positioned within the uterus and polymerizing said prepolymer or monomer.
8. The intrauterine contraceptive device of claim 1 wherein the sides of said body are generally parabolic in shape.
9. An intrauterine contraceptive device comprising: a preformed hollow body having a shape approximating an equilateral triangle with a continuous, imperforate top wall joined at its periphery to a continuous, imperforate bottom wall, said 'walls being formed of a thin, flexible material and being connected to each other at a plurality of spaced apart areas which extend inwardly from the side edges of said top and bottom walls to limit expansion of said body; means defining an opening in one of the apices of said hollow body for filling and emptying said hollow body; means closing said opening; and a flexible, compressible, filler material substantially completely filling said hollow body whereby the walls of said body will make contact with a major portion of the walls of said uterine cavity when said device is positioned in said uterine cavity.
10. An intrauterine contraceptive device comprising: a preformed hollow body having a shape approximating an equilateral triangle with a continuous, imperforate top wall joined at its periphery to a continuous, imperforate bottom wall, said walls being formed of a thin, flexible material and being connected to each other at a centrally located, triangularly shaped area to limit expansion of said body; means defining an openingin one of the apices of said hollow body for filling and emptying said hollow body; means closing said opening; and a flexible, compressible, filler material substantially completely filling said hollow body whereby the walls of said body will make contact with a major portion of the walls of said uterine cavity when said device is positioned in said uterine cavity.
11. An intrauterine contraceptive device comprising: a preformed hollow body having a shape approximating an equilateral triangle with a continuous, imperforate top wall joined at its periphery to a continuous, imperforate bottom wall, said walls being formed of a thin, flexible material and being connected to each other along at least two spaced apart lines extending inwardly from the top edge of said walls to limit expansion of said body; means defining an opening in one of the apices of said hollow body for filling and emptying said hollow body; means closing said opening; and a flexible, compressible, filler material substantially completely filling said hollow body whereby the walls of said body will make contact with a major portion of the walls of said uterine cavity when said device is positioned in said uterine cavity.
g g gg V UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 5,779, 41 Dated December 18, 1975 Inventor(s) William O. Vennard et a1 It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Column 1, line 57, reads "contractptive", should readcontraceptive Column 2, line 55, reads and", should read the Column 7,line 19, reads "is soluble", should read is substantially soluble Signed and sealed this 9th day of April 197A.
(SEAL) Attest:
C. MARSHALL DANN EDWARD II.IILETGHER,JR. Attesting Officer Commissioner of Patents

Claims (11)

1. An intrauterine contraceptive device comprising: a preformed hollow body having a shape approximating an equilateral triangle with a continuous, imperforate top wall joined at its periphery to a continuous, imperforate bottom wall, said walls being formed of a thin, flexible material and being connected to each other by connector stem means at one or more points intermediate their peripheries to limit expansion of said body; means defining an opening in one of the apices of said hollow body for filling and emptying said hollow body; means closing said opening; and a flexible, compressible, filler material substantially completely filling said hollow body whereby the walls of said body will make contact with a major portion of the walls of said uterine cavity when said device is positioned in said uterine cavity.
9. An intrauterine contraceptive device comprising: a preformed hollow body having a shape approximating an equilateral triangle with a continuous, imperforate top wall joined at its periphery to a continuous, imperforate bottom wall, said walls being formed of a thin, flexible material and being connected to each other at a plurality of spaced apart areas which extend inwardly from the side edges of said top and bottom walls to limit expansion of said body; means defining an opening in one of the apices of said hollow body for filling and emptying said hollow body; means closing said opening; and a flexible, compressible, filler material substantially completely filling said hollow body whereby the walls of said body will make contact with a major portion of the walls of said uterine cavity when said device is positioned in said uterine cavity.
11. An intrauterine contraceptive device comprising: a preformed hollow body having a shape approximating an equilateral triangle with a continuous, imperforate top wall joined at its periphery to a continuous, imperforate bottom wall, said walls being formed of a thin, flexible material and being connected to each other along at least two spaced apart lines extending inwardly from the top edge of said walls to limit expansion of said body; means defining an opening in one of the apices of said hollow body for filling and emptying said hollow body; means closing said opening; and a flexible, compressible, filler material substantially completely filling said hollow body whereby the walls of said body will make contact with a major portion of the walls of said uterine cavity when said device is positioned in said uterine cavity.
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US3867933A (en)*1973-03-061975-02-25Tecna CorpIntrauterine device and process of making the same
US3913573A (en)*1972-10-021975-10-21Morton GutnickIntrauterine contraceptive devices with plural parallel leg segments
US3923051A (en)*1974-03-181975-12-02Samuel SoichetInflatable intrauterine contraceptive device for postpartum use
US3933153A (en)*1974-03-181976-01-20Laszlo Kalman CsataryIntra-uterine contraceptive device
US3994291A (en)*1974-07-011976-11-30Saeed SalmasianSalmasian inflatable intra-uterine device
US3996933A (en)*1972-10-021976-12-14Morton GutnickIntrauterine contraceptive devices and processes
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US4363318A (en)*1979-12-311982-12-14University Patents, Inc.Custom valved cervical cap
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US20030032963A1 (en)*2001-10-242003-02-13Kyphon Inc.Devices and methods using an expandable body with internal restraint for compressing cancellous bone
US20030153940A1 (en)*2000-12-272003-08-14Martin NohillySurgical balloon having varying wall thickness
US20040153114A1 (en)*1994-01-262004-08-05Kyphon Inc.Inflatable device for use in surgical protocol relating to fixation of bone
US20050255039A1 (en)*1998-06-262005-11-17Pro Surg, Inc., A California CorporationGel injection treatment of breast, fibroids & endometrial ablation
US20080058857A1 (en)*1994-01-262008-03-06Kyphon, Inc.Systems and methods treating a vertebral body
US7967827B2 (en)1994-01-262011-06-28Kyphon SarlMethods and devices for treating fractured and/or diseased bone using an expandable structure that remains within the bone
US20130019374A1 (en)*2011-01-042013-01-24Schwartz Alan NGel-based seals and fixation devices and associated systems and methods
US10342476B2 (en)2012-05-172019-07-09Alan N. SchwartzLocalization of the parathyroid
US11045246B1 (en)2011-01-042021-06-29Alan N. SchwartzApparatus for effecting feedback of vaginal cavity physiology
US11337858B2 (en)2011-11-212022-05-24Alan N. SchwartzOstomy pouching system
US11406438B2 (en)2011-09-232022-08-09Alan N. SchwartzInstrument for therapeutically cytotoxically ablating parathyroidal tissue within a parathyroid gland

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US3996933A (en)*1972-10-021976-12-14Morton GutnickIntrauterine contraceptive devices and processes
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