Home › Device types › FZS
Curette, Surgical, General Use
FDA product code FZS · Class 1 · General, Plastic Surgery
8,557
Registered devices
71
Adverse events
3
Recalls
14
510(k) clearances
Devices with this code
AESCULAP — AESCULAP, INC.Curette — KOROS U.S.A., INC.Life Instruments — Life Instrument CorporationSurtex — SURTEX INSTRUMENTS LTD.Symmetry Karlin™ — ASPEN SURGICAL PRODUCTS, INC.Symmetry Karlin™ XL Magnum — ASPEN SURGICAL PRODUCTS, INC.Medfix — MEDFIX INTERNATIONAL, LLCSurtex — SURTEX INSTRUMENTS LTD.Life Instruments — Life Instrument CorporationAmbler Surgical — AMBLER SURGICAL CORP.TSI — TEDAN SURGICAL INNOVATIONS, L.L.C.gSource — GSOURCE LLCSklar® — SKLAR CORPORATIONHNM MEDICAL — HNM STAINLESS, LLC.gSource — GSOURCE LLCSurtex — SURTEX INSTRUMENTS LTD.Life Instruments — Life Instrument CorporationCurette — KOROS U.S.A., INC.Medtronic Reusable Instruments — MEDTRONIC SOFAMOR DANEK, INC.Life Instruments — Life Instrument CorporationMedtronic Reusable Instruments — MEDTRONIC SOFAMOR DANEK, INC.gSource — GSOURCE LLCSklar — SKLAR CORPORATIONCurette — KOROS U.S.A., INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
| 2013-11-05 | Zimmer, Inc. | Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that pr |
| 2011-07-15 | X Spine Systems Inc | The firm learned that the Torque Driver Handles were not actuating at a proper torque. It was determined that the handles were speed determinant and could outp |
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