Medical Device Manufacturer · US , Englewood , NJ

Foremost Dental Mfg., Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1985

Total

Cleared

Denied

Foremost Dental Mfg., Inc. has 14 FDA 510(k) cleared dental devices. Based in Englewood, US.

Historical record: 14 cleared submissions from 1985 to 1998.

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

Foremost Dental Mfg., 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 - Foremost Dental Mfg., Inc.

14 devices

1-12 of 14

Cleared Aug 10, 1998

ZENITH LUXACORE AUTOMIX CORE MATERIAL (MULTIPLE)

K982201 · EBF

Dental · 49d

Cleared Jul 10, 1998

PERMACEM AUTOMIX LUTING CEMENT SYSTEM

K981813 · EBF

Dental · 49d

Cleared May 11, 1998

HONIGUM AUTOMIX IMPRESSION MATERIAL (FOIL BAGS) AND HONIGUM QUICK IMPRESSION...

K980963 · ELW

Dental · 56d

Cleared Jul 15, 1997

ZENTIH FLOWABLE COMPOSITE (MULTIPLE)

K970683 · EBF

Dental · 141d

Cleared Jun 03, 1997

TEMPOCEM NE (MULTIPLE)

ZENITH TOTAL ETCH 10% PHOSPHORIC ACID

K935032 · EBF

Dental · 90d

Cleared Feb 13, 1989

ZENITH 40% PHOSPHORIC ACID GEL

FOREMOST DENTIN ADHESIVE

K864898 · EMA

Dental · 59d

Cleared Nov 19, 1985

LIGHT CURE FILLING MATERIAL

K853055 · EBF

Dental · 123d

Foremost Dental Mfg., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Foremost Dental Mfg., Inc.

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