Medical Device Manufacturer · US , Walker , MI

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

23 submissions · 23 cleared · Since 1981

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.

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

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