Home › Device types › NBH
Accessories, Arthroscopic
FDA product code NBH · Class 1 · Orthopedic
7,217
Registered devices
5,221
Adverse events
55
Recalls
2
510(k) clearances
Devices with this code
Arthrex® — ARTHREX, INC.ELITE — Smith & Nephew, Inc.NA — STRYKER CORPORATIONNA — Smith & Nephew, Inc.Y-KNOT — Conmed CorporationMillennium — Avalign Technologies, Inc.CROSSTRAC — Smith & Nephew, Inc.Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY, INC.Medline — MEDLINE INDUSTRIES, INC.NA — Smith & Nephew, Inc.Arthrex® — ARTHREX, INC.N/A — Smith & Nephew, Inc.ENDOTRIG — Stryker GmbHELMED — ELMED INCORPORATEDN/A — Smith & Nephew, Inc.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftStrauss Surgical — AMERICAN MEDICAL ENDOSCOPY, INC.N/A — Smith & Nephew, Inc.ENDOBUTTON — Smith & Nephew, Inc.Y-Knot, OneStep — Conmed CorporationSurgical Direct — Surgical Direct, Inc.ACUFEX — Smith & Nephew, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-09-21 | Smith & 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 |
| 2019-06-25 | BioPro, Inc. | Manufacturing flaw in the sterile barrier system |
| 2019-06-25 | BioPro, Inc. | Manufacturing flaw in the sterile barrier system |
| 2019-06-25 | BioPro, Inc. | Manufacturing flaw in the sterile barrier system |
| 2019-06-25 | BioPro, Inc. | Manufacturing flaw in the sterile barrier system |
| 2019-06-25 | BioPro, Inc. | Manufacturing flaw in the sterile barrier system |
| 2019-06-25 | BioPro, Inc. | Manufacturing flaw in the sterile barrier system |
| 2019-06-25 | BioPro, Inc. | Manufacturing flaw in the sterile barrier system |
| 2019-06-25 | BioPro, Inc. | Manufacturing flaw in the sterile barrier system |
| 2019-06-25 | BioPro, Inc. | Manufacturing flaw in the sterile barrier system |
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