Home › Device types › KOJ
Airbrush
FDA product code KOJ · Class 2 · Dental
157
Registered devices
19
Adverse events
1
Recalls
48
510(k) clearances
Devices with this code
Aurora™ — PARKELL, INC.MICROETCHER — DANVILLE MATERIALS, LLCParkell® — PARKELL, INC.LOVE HYGIENE — Guilin Woodpecker Medical Instrument Co., Ltd.Etchmaster — RELIANCE ORTHODONTIC PRODUCTS INCMB coupling Borden — DELDENT LTD.ETCHMASTER — RELIANCE ORTHODONTIC PRODUCTS INCEtchmaster — RELIANCE ORTHODONTIC PRODUCTS INCHuFriedyGroup — HU-FRIEDY MFG. CO., LLCSubgingival PWR Perio Tips — HU-FRIEDY MFG. CO., LLCJohnson-Promident — Young Innovations, Inc.ETCHMASTER — RELIANCE ORTHODONTIC PRODUCTS INCASK — RELIANCE ORTHODONTIC PRODUCTS INCASK — RELIANCE ORTHODONTIC PRODUCTS INCAIR-FLOW — E.M.S. Electro Medical Systems S.A.ETCHMASTER — RELIANCE ORTHODONTIC PRODUCTS INCHenry Schein — HENRY SCHEIN, INC.JETSTREAM — DELDENT LTD.Etchmaster — RELIANCE ORTHODONTIC PRODUCTS INCETCHMASTER — RELIANCE ORTHODONTIC PRODUCTS INCEtchmaster — GROMAN INC.DTE — Guilin Woodpecker Medical Instrument Co., Ltd.CoJet™ — 3M Deutschland GmbHEtchmaster — GROMAN INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-12-13 | Groman Inc. | Groman Inc. of Margate, FL recalled their product Cordless Etcher Air Brush. When non-conforming cartridges are inserted into the Cordless Etcher they can induc |
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.
