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Forceps
FDA product code HTD · Class 1 · General, Plastic Surgery
9,565
Registered devices
2,217
Adverse events
14
Recalls
73
510(k) clearances
Devices with this code
Lahey Forceps — SONTEC INSTRUMENTS, INC.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.ASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATIONMSI Precision Specialty Instruments — Med Saver, Inc.AESCULAP — Aesculap AGdevemed — devemed GmbHCOOLEY TYING FORCEPS — SONTEC INSTRUMENTS, INC.Yasargil Forceps — SONTEC INSTRUMENTS, INC.MSI Precision Specialty Instruments — Med Saver, Inc.HNM Medical — HNM STAINLESS, LLC.HNM Medical — HNM STAINLESS, LLC.PRINCETON — Princeton Medical Group, Inc.NORDENT MANUFACTURING INC — NORDENT MANUFACTURING INCSurgical Direct — Surgical Direct, Inc.EXPEDIUM — Medos International SàrlWexler Surgical, Inc. — WEXLER SURGICAL, INC.Tecomet — TECOMET INC.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.Wexler Surgical, Inc. — WEXLER SURGICAL, INC.NA — Synthes GmbHWexler Surgical, Inc. — WEXLER SURGICAL, INC.Wexler Surgical, Inc. — WEXLER SURGICAL, INC.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.Surgical Direct — Surgical Direct, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
| 2022-07-25 | Stradis Medical, LLC dba Stradis Healthcare | The sterile barrier may be compromised. |
| 2022-07-25 | Stradis Medical, LLC dba Stradis Healthcare | The sterile barrier may be compromised. |
| 2019-01-09 | ConvaTec, Inc | An internal assessment of packaging confirmed the potential for a breach in the sterile barrier. |
| 2018-11-02 | Baxter Healthcare Corporation | Potential presence of rust on Coupler Forceps (GEM4183C). |
| 2013-11-26 | Biomet, Inc. | Inner label of PN: 906768 Lot: 055450 CurvTek Eye Needle 22mm X-Large states incorrectly PN: 906760 7mm Medium. |
| 2013-11-20 | Edwards Lifesciences, LLC | Edwards Lifesciences is recalling one lot of Ergonic instrument due to mislabeling. Ergonic scissors standard curved labeled as a Double Acting DeBakey forcep. |
| 2009-09-03 | Synthes USA (HQ), Inc. | The recalling firm has determined that the customized plates instruments do not have a cleared premarket notification. |
| 2009-09-03 | Synthes USA (HQ), Inc. | The recalling firm has determined that the customized plates instruments do not have a cleared premarket notification. |
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