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Pliers, Surgical
FDA product code HTC · Class 1 · General, Plastic Surgery
1,136
Registered devices
412
Adverse events
4
Recalls
10
510(k) clearances
Devices with this code
MSI Precision Specialty Instruments — Med Saver, Inc.Forcep — KOROS U.S.A., INC.Forcep — KOROS U.S.A., INC.Novo Surgical Inc. — NOVO SURGICAL, INC.KMEDIC — TELEFLEX INCORPORATEDSalvin Dental Specialties — SALVIN DENTAL SPECIALTIES, LLCMillennium — Avalign Technologies, Inc.Evos Mini — Smith & Nephew, Inc.Symmetry Surgical — ASPEN SURGICAL PRODUCTS, INC.MCI - Medical Concept Innovation, Inc. — MCI-MEDICAL CONCEPT INNOVATION INCSymmetry Surgical — ASPEN SURGICAL PRODUCTS, INC.AESCULAP — Aesculap AGZOLL-DENTAL — Zoll-DentalForcep — KOROS U.S.A., INC.ELMED — ELMED INCORPORATEDZOLL-DENTAL — Zoll-DentalForceps — KOROS U.S.A., INC.MEMBRANE FORCEPS 14cm 6X10mm — W.H. Holden, Inc.MSI Precision Specialty Instruments — Med Saver, Inc.Salvin Dental Specialties — SALVIN DENTAL SPECIALTIES, LLCTecomet — TECOMET INC.ZOLL-DENTAL — Zoll-DentalForcep — KOROS U.S.A., INC.HELMUT ZEPF — Helmut Zepf Medizintechnik GmbH
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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