Genoss Co., Ltd.
Genoss Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2025.
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.