Medical Device Manufacturer · US , Walker , MI

G-C Intl. Corp. - FDA 510(k) Cleared Devices

23 submissions · 23 cleared · Since 1981

Recent clearances: MIRACLE MIX CAPS GLASS IONOMER CEMENT INCAPSULES, FUJI II LC, FUJI LINING CEMENT LIGHT CURE

Total

Cleared

Denied

G-C Intl. Corp. has 23 FDA 510(k) cleared dental devices. Based in Walker, US.

Historical record: 23 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.

G-C Intl. Corp. 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 - G-C Intl. Corp.

23 devices

1-12 of 23

Cleared Dec 27, 1991

MIRACLE MIX CAPS GLASS IONOMER CEMENT INCAPSULES

FUJI LINING CEMENT LIGHT CURE

K901999 · EJK

Dental · 90d

Cleared Jul 13, 1990

EXAPHASE, SINGLE PHASE IMPRESSION MATERIAL

RESUBMITTED EMA DENTIN CEMENT

K883770 · EMA

Dental · 85d

Cleared May 16, 1988

FUJI CAP II CAPSULE & APPLIER

G-C Intl. Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - G-C Intl. Corp.

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