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Clamp
FDA product code HXD · Class 1 · General, Plastic Surgery
2,420
Registered devices
1,235
Adverse events
4
Recalls
14
510(k) clearances
Devices with this code
DeBakey Derra Anastomosis Clamps — KOROS U.S.A., INC.Ambler Surgical — AMBLER SURGICAL CORP.MSI Precision Specialty Instruments — Med Saver, Inc.Ambler Surgical — AMBLER SURGICAL CORP.N/A — BLACK & BLACK SURGICAL, INC.Innomed, Inc. — INNOMED, INC.PILLING — TELEFLEX INCORPORATEDInnomed, Inc. — INNOMED, INC.Innomed, Inc. — INNOMED, INC.Doyen Intestinal Forceps — SONTEC INSTRUMENTS, INC.Innomed, Inc. — INNOMED, INC.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.GEN2 — SURGIX MEDICAL LLCINSTRUMENT — Howmedica Osteonics Corp.L-Box® — INNO Holdings, Inc.WANClamp,EndoEZ Clamp — Well Lead Medical Co.,LtdNovo Surgical — NOVO SURGICAL, INC.ORTHOMED — ORTHO-MED, INC.PEAK MEDICAL — Peak Medical Distribution Inc.Hayden Medical — Hayden Medical, Inc.LAZIC — Peter Lazic GmbHINSTRUMENT — Howmedica Osteonics Corp.AESCULAP — Aesculap AGAvalign — Avalign Technologies, 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. |
| 2024-02-23 | MEDLINE INDUSTRIES, LP - Northfield | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. |
| 2018-05-04 | Stryker GmbH | Laser etching which indicates whether the device is in compression or distraction mode appears to be on the wrong side of the lever arm |
| 2015-06-16 | Symmetry Surgical, Inc. | Lack of sterility assurance. |
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