Medical Device Manufacturer · DE , West Germany

Degussa AG - FDA 510(k) Cleared Devices

33 submissions · 33 cleared · Since 1990

Total

Cleared

Denied

Degussa AG has 33 FDA 510(k) cleared dental devices. Based in West Germany, DE.

Historical record: 33 cleared submissions from 1990 to 1995.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Degussa AG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Degussa AG

33 devices

1-12 of 33

DUCERAGOLD, DUCERATIN

DUCERATIN/DUCERAM LFC DENTAL PORCELAIN

PART 872 DEGUFILL H & DEGUFILL M DA

K914368 · EKJ

Dental · 43d

Cleared Nov 07, 1991

DENTOMAT 3 AMALGAMATORS

K914339 · EFD

Dental · 41d

Degussa AG - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Degussa AG

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