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

1-23 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-CERA PORCELAIN BOND

K880765 · EBF

Dental · 52d

Cleared Apr 12, 1988

G-CERA PORCELAIN & G-CERA PORCELAIN MODIFIER

76 ELW BITE CHECKER SILICONE

EXAFLEX IMPRESSION MATERIAL

K812406 · ELW

Dental · 46d

Cleared Oct 06, 1981

G-C FIT-CHECKER IMPRESSION MATERIAL

K812679 · ELW

Dental · 14d

Cleared Oct 06, 1981

G-C IMPRESSION SYRINGE

FUJI IONOMER TYPE I & II

K811521 · EMA

Dental · 28d

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

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