Genoss Co., Ltd.
FDA 510(k) medical device clearances.
Top product codes for Genoss Co., Ltd.
Recent clearances by Genoss Co., Ltd.
- K242386 — Bluemoon
- K222688 — The Trust
- K233885 — rainbow Paste Stain SE
- K232174 — rainbowTM Multi-Layer Block / bright 3-Layer / bright Mono
- K231480 — Bright MTA Sealer Plus
- K214086 — Bright Impress-Light, Bright Impress-Medium, Bright Impress-Heavy, Bright Impress-Bite, Bright Impress-Putty
- K200155 — Bright High Flow
- K200153 — Bright Bond Universal
- K200156 — Bright Low Flow
- K170596 — TN-Brush
- K160079 — rainbow Shine
- K153676 — OSTEON III
- K160144 — rainbow LS Block
- K112716 — OSTEON II
- K102307 — GENOSS COLLAGEN MEMBRANE MODEL GCM1020, GCM3040 TOTAL 6 MODELS
- K102015 — OSTEON, OSTEON SINUS, OSTEON LIFTING
- K092513 — RAINBOW BLOCK
- K062834 — OSTEON, MODELS GBG0305, GBG0510, GBG1020, GBG2030, GBG3040, GBG4050
Data sourced from openFDA. This site is unofficial and independent of the FDA.