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Pliers, Surgical
FDA product code HTC · Class 1 · General, Plastic Surgery
1,087
Registered devices
412
Adverse events
4
Recalls
10
510(k) clearances
Devices with this code
BR Surgical, LLC — BR Surgical, LLCORTHOMED — ORTHO-MED, INC.Novo Surgical Inc. — NOVO SURGICAL, INC.MEMBRANE FORCEPS 14cm 3X6mm — W.H. Holden, Inc.KOHDENT — Kohler Medizintechnik GmbHMedtronic Reusable Instruments — MEDTRONIC SOFAMOR DANEK, INC.Symmetry Surgical — ASPEN SURGICAL PRODUCTS, INC.EVOS — Smith & Nephew, Inc.NA — Synthes GmbHHELMUT ZEPF — Helmut Zepf Medizintechnik GmbHMSI Precision Specialty Instruments — Med Saver, Inc.Innomed, Inc. — INNOMED, INC.PLIERS — KLS-Martin L.P.BENCO — BENCO DENTAL SUPPLY CO.Total Foot System 2 — Smith & Nephew, Inc.Novo Surgical Inc. — NOVO SURGICAL, INC.Forcep — KOROS U.S.A., INC.Symmetry Surgical — ASPEN SURGICAL PRODUCTS, INC.Novo Surgical Inc. — NOVO SURGICAL, INC.MCI - Medical Concept Innovation, Inc. — MCI-MEDICAL CONCEPT INNOVATION INCBR Surgical, LLC — BR Surgical, LLCKOHDENT — Kohler Medizintechnik GmbHKOHDENT — Kohler Medizintechnik GmbHFAICO CMF System — FAICO MEDICAL LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-11-14 | The Anspach Effort, Inc. | May operate solely in reverse mode, not operate in reverse mode when intended, not function or an unintentionally start. |
| 2014-11-06 | Synthes (USA) Products LLC | The device may operate solely in reverse mode, not operate in reverse mode when intended, not function, or unintentionally start. Unintended start of the hand |
| 2014-08-14 | The Anspach Effort, Inc. | The affected Small Electric Drive (SED) may operate solely in reverse mode, not operate in reverse mode when intended, not function, or unintentionally start. |
| 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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