Medical Device Manufacturer · US , Mchenry , IL

Sybron Corp. - FDA 510(k) Cleared Devices

37 submissions · 37 cleared · Since 1977

37

Total

37

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sybron Corp. Dental ✕

13 devices

1-12 of 13

Cleared Jun 23, 1986

Cleared Jan 30, 1986

PROOF ALGINATE IMPRESSION MATERIAL

Cleared Jul 13, 1984

KERR SEALAPEX ROOT CANAL SEALER

Cleared May 21, 1984

KERR RESIN BONDED BRIDGE CEMENT

Cleared Jan 26, 1983

EVERBOND GLASS IONOMER CEMENT

Cleared Oct 13, 1982

COMMAND BONDING RESIN/GLAZE/OPAQUER

Cleared Mar 02, 1982

SYBRON/KERR COMMAND

Cleared Feb 24, 1982

SYBRON/KERR CONTOUR

Cleared Feb 24, 1982

SYBRON/KERR MIRROR 3

Cleared Jun 26, 1981

Cleared Aug 04, 1980

KERR CORE COMPOSITE

Cleared Jul 28, 1980