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Diaphragm, Contraceptive (And Accessories)
FDA product code HDW · Class 2 · Obstetrics/Gynecology
19
Registered devices
44
Adverse events
3
Recalls
4
510(k) clearances
Devices with this code
Omniflex Diaphragm — Coopersurgical, Inc.Omniflex Diaphragm — Coopersurgical, Inc.Omniflex Diaphragm — Coopersurgical, Inc.Arcing Diaphragm — Coopersurgical, Inc.Milex — Coopersurgical, Inc.Omniflex Diaphragm — Coopersurgical, Inc.Milex — Coopersurgical, Inc.Arcing Diaphragm — Coopersurgical, Inc.Caya contoured diaphragm — KESSEL medintim GmbHOmniflex Diaphragm — Coopersurgical, Inc.Omniflex Diaphragm — Coopersurgical, Inc.Arcing Diaphragm — Coopersurgical, Inc.Omniflex Diaphragm — Coopersurgical, Inc.Arcing Diaphragm — Coopersurgical, Inc.Arcing Diaphragm — Coopersurgical, Inc.Arcing Diaphragm — Coopersurgical, Inc.Arcing Diaphragm — Coopersurgical, Inc.Omniflex Diaphragm — Coopersurgical, Inc.Arcing Diaphragm — Coopersurgical, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-02-16 | CooperSurgical, Inc. | The products have been identified to contain an incorrect size Diaphragm. |
| 2015-05-20 | CooperSurgical, Inc. | A diaphragm size 80 labeled box was incorrectly packaged with a size 85. |
| 2013-02-26 | Cooper Surgical, Inc. | Incorrect size was printed on the outer product packaging. |
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