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Curette
FDA product code HTF · Class 1 · General, Plastic Surgery
5,501
Registered devices
117
Adverse events
2
Recalls
3
510(k) clearances
Devices with this code
TWO HANDED CURETTE — SONTEC INSTRUMENTS, INC.ENDOSKELETON® TT — MEDTRONIC SOFAMOR DANEK, INC.CONCORDE — DEPUY SPINE, LLCNA — Zimmer, Inc.Intervertebral Disc Preparation Instruments — ALPHATEC SPINE, INC.IdentiTi — ALPHATEC SPINE, INC.NA — DEPUY SPINE, LLCNA — Synthes GmbHZyston Interbody Spacer System — Highridge Medical, LLCMSI Precision Specialty Instruments — Med Saver, Inc.NA — Synthes GmbHN/A — GEORGE TIEMANN & CO.N/A — GEORGE TIEMANN & CO.Intervertebral Disc Preparation Instruments — ALPHATEC SPINE, INC.Disc Preparation Instruments — Highridge Medical, LLCHouse Curette — SONTEC INSTRUMENTS, INC.Battalion — ALPHATEC SPINE, INC.Quinelato — Schobell Industrial LtdaBattalion — ALPHATEC SPINE, INC.ORTHOMED — ORTHO-MED, INC.Ambler Surgical — AMBLER SURGICAL CORP.Cup Curette with Teeth Straight — CAPTIVA SPINE, INC.N/A — GEORGE TIEMANN & CO.n/a — MEDTRONIC SOFAMOR DANEK, INC.
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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