Home › Device types › EMO
Knife, Periodontic
FDA product code EMO · Class 1 · Dental
379
Registered devices
0
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
HU-FRIEDY — HU-FRIEDY MFG. CO., LLCOtto Leibinger — AMERICAN EAGLE INSTRUMENTS, INC.PA TUNNELING INSTRUMENT #4 D/E DLC HF HANDLE — W.H. Holden, Inc.Darby Dental Supply, LLC — DARBY DENTAL SUPPLY, LLCOSUNG MND — OSUNG MND Co., Ltd.Laschal Surgical — LASCHAL SURGICAL INSTRUMENTS, INCBrasseler USA — Peter Brasseler Holdings, LLCNORDENT MANUFACTURING INC — NORDENT MANUFACTURING INC4-B LONG DLC — W.H. Holden, Inc.PERIO KNIFE GOLDMAN FOX 11 CH HANDLE — W.H. Holden, Inc.1-A MEDIUM DLC — W.H. Holden, Inc.STOMA® — Storz am Mark GmbHAmerican Eagle Instruments — AMERICAN EAGLE INSTRUMENTS, INC.Leetrac Wide Blade — B& L Biotech, inc.PERIO KNIFE GOLDMAN FOX 7 HF HANDLE — W.H. Holden, Inc.KNIFE — KLS-Martin L.P.Laschal Surgical — LASCHAL SURGICAL INSTRUMENTS, INC4-A MEDIUM DLC — W.H. Holden, Inc.PA TUNNELING INSTRUMENT #2 D/E HF HANDLE — W.H. Holden, Inc.ZOLL-DENTAL — Zoll-DentalLeetrac Wide handle — B& L Biotech, inc.VESTIBULAR TUNNELING ELEVATOR #4 D/E HF HANDLE — W.H. Holden, Inc.VESTIBULAR TUNNELING ELEVATOR #6 D/E HF HANDLE — W.H. Holden, Inc.PA TUNNELING INSTRUMENT #3 D/E HF HANDLE — W.H. Holden, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-03-28 | Ace Surgical Supply Co., Inc. | The product inside the package is incorrect. A single blade shoe was mistakenly packaged instead of a double blade. |
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.
