G-C Intl. Corp.
G-C Intl. Corp. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 1991.
Top product codes for G-C Intl. Corp.
Recent clearances by G-C Intl. Corp.
- K913175 — MIRACLE MIX CAPS GLASS IONOMER CEMENT INCAPSULES
- K913884 — FUJI II LC
- K901999 — FUJI LINING CEMENT LIGHT CURE
- K902531 — EXAPHASE, SINGLE PHASE IMPRESSION MATERIAL
- K896883 — GC CERVICAL CEMENT
- K895976 — TOOTH SHADE RESIN
- K892806 — TUF-COAT
- K890830 — DENTURE RESIN
- K890829 — UNIFAST LC
- K883770 — RESUBMITTED EMA DENTIN CEMENT
- K880848 — FUJI CAP II CAPSULE & APPLIER
- K880849 — EXAMIX DISPENSER
- K880765 — G-CERA PORCELAIN BOND
- K880764 — G-CERA PORCELAIN & G-CERA PORCELAIN MODIFIER
- K851468 — 76 EMA LINING CEMENT
- K851469 — 76 ELW BITE CHECKER SILICONE
- K844653 — LIMI ALLOY
- K844329 — SURFLEX F
- K812406 — EXAFLEX IMPRESSION MATERIAL
- K812679 — G-C FIT-CHECKER IMPRESSION MATERIAL
- K812680 — G-C IMPRESSION SYRINGE
- K812568 — CAVITRON
- K811521 — FUJI IONOMER TYPE I & II
Data sourced from openFDA. This site is unofficial and independent of the FDA.