Home › Device types › FZS
Curette, Surgical, General Use
FDA product code FZS · Class 1 · General, Plastic Surgery
7,919
Registered devices
71
Adverse events
3
Recalls
14
510(k) clearances
Devices with this code
Anatomic Access LLIF — Tyber Medical, LLCGen2 — SURGIX MEDICAL LLCTSPACE — Aesculap AGLAZIC — Peter Lazic GmbHLife Instruments — Life Instrument CorporationIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONGen2 — SURGIX MEDICAL LLCSymmetry Surgical — ASPEN SURGICAL PRODUCTS, INC.Life Instruments — Life Instrument CorporationLife Instruments — Life Instrument CorporationPRINCETON — Princeton Medical Group, Inc.BR Surgical, LLC — BR Surgical, LLCLife Instruments — Life Instrument CorporationLife Instruments — Life Instrument CorporationLife Instruments — Life Instrument CorporationMedtronic Reusable Instruments — MEDTRONIC SOFAMOR DANEK, INC.VertebraLINK — LINKSPINE, INC.Curette — KOROS U.S.A., INC.ELITE MEDICAL INSTRUMENTATION — ELITE MEDICAL INSTRUMENTATIONLife Instruments — Life Instrument CorporationGen2 — SURGIX MEDICAL LLCGen2 — SURGIX MEDICAL LLCAESCULAP — AESCULAP, INC.Sklar® — SKLAR CORPORATION
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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