GC America, Inc.
GC America, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2026.
Clearances by GC America, Inc. — page 2
101–129 of 129- K982695 — GC RELINE
- K981461 — GC FUJI ORTHO LC
- K981514 — GC FUJI BOND LC
- K981370 — MIRACLE MIX CAPSULE
- K980695 — FUJI I
- K980682 — FUJI II
- K973343 — HYDROFLEX
- K972594 — METALPRIMER II
- K970656 — HYDROFLEX
- K963144 — GC BASELINE
- K961448 — FUJI IX GP
- K961417 — GC FUJI ORTHO
- K961584 — FUJI II LC (IMPROVED)
- K955932 — EXAFLEX IMPRESSION MATERIAL (MODIFICATION)
- K953166 — FUJI BOND LC
- K951555 — FUJI IX
- K950556 — FUJI ORTHO LC
- K942993 — THERMORESIN LC II
- K946100 — FUJI DUET
- K942670 — GC PATTERN RESIN
- K943388 — GC SURFLEX F
- K940565 — COE-SOFT LC
- K935961 — GC FUJI COAT LC
- K935960 — GC TEMPRON
- K935261 — KOOLINER II
- K930939 — REBARON LC
- K935521 — GC ELITE CEMENT
- K933206 — EXA BITE REGISTRATION MATERIAL
- K932039 — G-CERA ORBIT COLOUR COMMUNICATION SET
Data sourced from openFDA. This site is unofficial and independent of the FDA.