Foremost Dental Mfg., Inc.
Foremost Dental Mfg., Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1998.
Top product codes for Foremost Dental Mfg., Inc.
Recent clearances by Foremost Dental Mfg., Inc.
- K982201 — ZENITH LUXACORE AUTOMIX CORE MATERIAL (MULTIPLE)
- K981813 — PERMACEM AUTOMIX LUTING CEMENT SYSTEM
- K980963 — HONIGUM AUTOMIX IMPRESSION MATERIAL (FOIL BAGS) AND HONIGUM QUICK IMPRESSION MATERIAL (CARTRIDGES)
- K970683 — ZENTIH FLOWABLE COMPOSITE (MULTIPLE)
- K970774 — TEMPOCEM NE (MULTIPLE)
- K970775 — TEMPO CEM (MULTIPLE)
- K954867 — IONOSIT SEAL
- K935032 — ZENITH TOTAL ETCH 10% PHOSPHORIC ACID
- K890464 — ZENITH 40% PHOSPHORIC ACID GEL
- K871562 — IONOCAL
- K864898 — FOREMOST DENTIN ADHESIVE
- K853055 — LIGHT CURE FILLING MATERIAL
- K845033 — FOREMOST DENTIN ADHESIVE
- K845034 — FOREMOST LITE CURE PIT & FISSURE SEALANT
Data sourced from openFDA. This site is unofficial and independent of the FDA.