FDA Device Intelligence
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Forceps, Biopsy, Gynecological

FDA product code HFB · Class 1 · Obstetrics/Gynecology

1,004
Registered devices
61
Adverse events
1
Recalls
22
510(k) clearances

Devices with this code

Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONV. Mueller — STERIS CORPORATIONELITE MEDICAL INSTRUMENTATION — ELITE MEDICAL INSTRUMENTATIONBABY TISCHLER BIOPSY PUNCH 10" — BIOPSY FINE CUT INSTRUMENTSELMED — ELMED INCORPORATEDEndoch — Endoch IncHayden Medical — Hayden Medical, Inc.Symmetry Surgical — ASPEN SURGICAL PRODUCTS, INC.Endoch — Endoch IncAESCULAP — Aesculap AGNovo Surgical Inc. — NOVO SURGICAL, INC.Hayden Medical — Hayden Medical, Inc.Endoch — Endoch IncMarina Medical — MARINA MEDICAL INSTRUMENTS, INC.RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHUTERINE BIOPSY PUNCH — SONTEC INSTRUMENTS, INC.Hayden Medical — Hayden Medical, Inc.Endoch — Endoch IncNovo Surgical — NOVO SURGICAL, INC.BR Surgical, LLC — BR Surgical, LLCHNM MEDICAL — HNM STAINLESS, LLC.Ambler Surgical — AMBLER SURGICAL CORP.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATION

Recent recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.