Medical Device Manufacturer · US , Mchenry , IL

Kulzer, Inc. - FDA 510(k) Cleared Devices

31 submissions · 31 cleared · Since 1981

Total

Cleared

Denied

Kulzer, Inc. has 31 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 31 cleared submissions from 1981 to 1991.

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

Kulzer, 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 - Kulzer, Inc.

31 devices

1-12 of 31

PALAPRESS(R) VARIO RESIN

K902115 · EBI

Dental · 78d

Cleared Jul 26, 1990

PALATRAY LC RESIN IMPRESSION TRAY MATERIAL

FORMASIL(R)A POLYVINYL SILOXANE LINE

K901681 · ELW

Dental · 65d

Kulzer, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Kulzer, Inc.

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