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Curette
FDA product code HTF · Class 1 · General, Plastic Surgery
5,325
Registered devices
116
Adverse events
2
Recalls
3
510(k) clearances
Devices with this code
Timberline Lateral Fusion System — Highridge Medical, LLCKMEDIC — TELEFLEX INCORPORATEDZyston Interbody Spacer System — Highridge Medical, LLCMillennium — Avalign Technologies, Inc.BAYONET RING CURETTE — SONTEC INSTRUMENTS, INC.General Instruments — ALPHATEC SPINE, INC.SOLITAIRE CERVICAL SPACER SYSTEM — Highridge Medical, LLCHELMUT ZEPF — Helmut Zepf Medizintechnik GmbHIntervertebral Disc Preparation Instruments — ALPHATEC SPINE, INC.Specials — Seaspine Orthopedics CorporationPLIF Allograft — Seaspine Orthopedics CorporationN/A — GEORGE TIEMANN & CO.IdentiTi — ALPHATEC SPINE, INC.NA — Zimmer, Inc.n/a — MEDTRONIC SOFAMOR DANEK, INC.Zyston Interbody Spacer System — Highridge Medical, LLCIntervertebral Body Fusion Device — PRECISION SPINE, INC.Curette — Zimmer GmbHHELMUT ZEPF — Helmut Zepf Medizintechnik GmbHRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHAmbler Surgical — AMBLER SURGICAL CORP.ENDOSKELETON® TT — MEDTRONIC SOFAMOR DANEK, INC.ASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATIONGENERIC Surgical Instruments — CTL Medical Corporation
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-11-12 | MEDLINE INDUSTRIES, LP - Northfield | Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection. |
| 2024-02-23 | MEDLINE INDUSTRIES, LP - Northfield | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. |
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