Medical Device Manufacturer · US , Mchenry , IL

Vivadent (Usa), Inc. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1978

17

Total

17

Cleared

0

Denied

Vivadent (Usa), Inc. has 17 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 17 cleared submissions from 1978 to 1986.

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

Vivadent (Usa), Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Vivadent (Usa), Inc.

17 devices

1-17 of 17

Cleared Oct 14, 1986

VIVADENT FILPIN

Cleared Jan 21, 1983

HELIOSIT-ORTHODONTIC

Ophthalmic · 67d

Cleared Dec 02, 1981

Cleared Dec 17, 1980

Cleared Nov 24, 1980

Cleared Nov 24, 1980

Cleared Nov 24, 1980

Cleared Nov 24, 1980

Cleared Nov 12, 1980

Cleared Nov 12, 1980

Cleared Aug 12, 1980

Cleared Jun 04, 1980

BONDALCAP (SILICO-PHOSPHATE)

Cleared Jun 04, 1980

BONDALCAP (CARBOXYLATE)

Cleared Jun 05, 1979

AMALCAP-NON-GAMMA-2

Cleared Apr 10, 1979

Cleared Apr 10, 1979

Cleared Dec 20, 1978