FDA Device Intelligence
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Accessories, Arthroscopic

FDA product code NBH · Class 1 · Orthopedic

7,185
Registered devices
5,126
Adverse events
55
Recalls
2
510(k) clearances

Devices with this code

N/A — Smith & Nephew, Inc.MEDLINE — MEDLINE INDUSTRIES, INC.CONMED — Conmed CorporationDOUBLELATCH — Conmed CorporationArthrex® — ARTHREX, INC.Tecomet — TECOMET INC.Arthrex — ProvisionNA — STRYKER CORPORATIONNA — Richard Wolf GmbHArthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.CONMED — Conmed CorporationReprocessed 2.9mm Tricut Blade, Rotatable — SURETEK MEDICALReprocessed 3.5mm Skimmer Angle Tip Blade, 18cm — SURETEK MEDICALArthrex® — ARTHREX, INC.Medline — MEDLINE INDUSTRIES, INC.Arthrex® — ARTHREX, INC.Surgical Direct — Surgical Direct, Inc.NA — Medos International SàrlNA — Smith & Nephew, Inc.NA — Smith & Nephew, Inc.N/A — Henke-Sass, Wolf GmbH

Recent recalls

DateFirmReason
2020-09-21Smith & Nephew, Inc.The J Lock feature on the cannula body was manufactured incorrectly, preventing the cannula from locking into an irrigation extender or arthroscope in the corre
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.