Home › Device types › EKH
Carver, Dental Amalgam, Operative
FDA product code EKH · Class 1 · Dental
918
Registered devices
17
Adverse events
1
Recalls
3
510(k) clearances
Devices with this code
PDT, Inc. — PDT, INC.Power Dental USA — Power Dental U.S.A. Inc.J & J INSTRUMENTS — J & J INSTRUMENTS INCSklar® — SKLAR CORPORATIONAmerican Eagle Instruments — AMERICAN EAGLE INSTRUMENTS, INC.HU-FRIEDY — HU-FRIEDY MFG. CO., LLCPDT, Inc. — PDT, INC.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONAESCULAP — Aesculap AGA. Titan Instruments — A. TITAN INSTRUMENTS, INC.NORDENT MANUFACTURING INC — NORDENT MANUFACTURING INCNORDENT MANUFACTURING INC — NORDENT MANUFACTURING INCReicodent — devemed GmbHHU-FRIEDY — HU-FRIEDY MFG. CO., LLCAmerican Eagle Instruments — AMERICAN EAGLE INSTRUMENTS, INC.HU-FRIEDY — HU-FRIEDY MFG. CO., LLCNORDENT MANUFACTURING INC — NORDENT MANUFACTURING INCAmerican Eagle Instruments — AMERICAN EAGLE INSTRUMENTS, INC.ZOLL-DENTAL — Zoll-DentalNORDENT MANUFACTURING INC — NORDENT MANUFACTURING INCReicodent — devemed GmbHHU-FRIEDY — HU-FRIEDY MFG. CO., LLCZOLL-DENTAL — Zoll-DentalA. Titan Instruments — A. TITAN INSTRUMENTS, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-04-20 | Almore International Inc | Microfil Composite Instruments were distributed with a sterile symbol on their packaging label inserts, indicating that the products are sold as sterile devices |
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