Home › Device types › EMF
Knife, Surgical
FDA product code EMF · Class 1 · General, Plastic Surgery
1,146
Registered devices
82
Adverse events
9
Recalls
21
510(k) clearances
Devices with this code
Gimmi — Gimmi GmbHSURGISTAR — SURGISTAR, INC.AESCULAP — Aesculap AGIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONZOLL-DENTAL — Zoll-DentalHU-FRIEDY — HU-FRIEDY MFG. CO., LLCLAZIC — Peter Lazic GmbHAmerican Medicals — American MedicalsSURGISTAR, INC. — SURGISTAR, INC.MicroAire® — Microaire Surgical Instruments LLCSURGISTAR — SURGISTAR, INC.LAZIC — Peter Lazic GmbHAESCULAP — Aesculap AGLAZIC — Peter Lazic GmbHAvalign — Avalign Technologies, Inc.SURGISTAR — SURGISTAR, INC.SURGISTAR — SURGISTAR, INC.SURGISTAR — SURGISTAR, INC.V. Mueller — STERIS CORPORATIONMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftMillennium — Avalign Technologies, Inc.Snowden-Pencer — STERIS CORPORATIONAESCULAP — AESCULAP, INC.Millennium — Avalign Technologies, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-05-07 | MicroAire Surgical Instruments, LLC | Potential that the blade can unintentionally cut tissue prior to the user deploying the blade. |
| 2020-05-18 | Carefusion 2200 Inc | Becton Dickinson and Company, is conducting a voluntary recall on the V. MuellerTM 3H Knife Handles catalog number listed in the table above. BD has been inform |
| 2018-05-14 | Beaver Visitec | Blades are loose in handles and may fall out due to non cured epoxy |
| 2017-11-03 | Beaver-Visitec International Inc. | The protective shield was retracted, and the blade was exposed. |
| 2017-11-03 | Beaver-Visitec International Inc. | The protective shield was retracted, and the blade was exposed. |
| 2017-11-03 | Beaver-Visitec International Inc. | The protective shield was retracted, and the blade was exposed. |
| 2017-11-03 | Beaver-Visitec International Inc. | The protective shield was retracted, and the blade was exposed. |
| 2017-11-03 | Beaver-Visitec International Inc. | The protective shield was retracted, and the blade was exposed. |
| 2013-05-03 | Surgical Instrument Service And Savings, Inc. | The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.