Genoss Co., Ltd. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Genoss Co., Ltd. has 18 FDA 510(k) cleared dental devices. Based in Laguna Niguel, US.
Latest FDA clearance: May 2025. Active since 2007.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
18 devices
Cleared
May 05, 2025
Bluemoon
Dental
266d
Cleared
Aug 09, 2024
The Trust
Dental
703d
Cleared
Jun 21, 2024
rainbow Paste Stain SE
Dental
196d
Cleared
Feb 23, 2024
rainbowTM Multi-Layer Block / bright 3-Layer / bright Mono
Dental
217d
Cleared
Jul 28, 2023
Bright MTA Sealer Plus
Dental
67d
Cleared
Dec 15, 2022
Bright Impress-Light, Bright Impress-Medium, Bright Impress-Heavy, Bright...
Dental
353d
Cleared
Nov 30, 2020
Bright High Flow
Dental
313d
Cleared
Oct 28, 2020
Bright Bond Universal
Dental
280d
Cleared
Oct 27, 2020
Bright Low Flow
Dental
279d
Cleared
Sep 11, 2017
TN-Brush
Dental
195d
Cleared
Nov 10, 2016
rainbow Shine
Dental
301d
Cleared
Sep 14, 2016
OSTEON III
Dental
268d
Cleared
Jul 21, 2016
rainbow LS Block
Dental
182d
Cleared
Jan 17, 2012
OSTEON II
Dental
120d
Cleared
May 04, 2011
GENOSS COLLAGEN MEMBRANE MODEL GCM1020, GCM3040 TOTAL 6 MODELS
Dental
261d
Cleared
Nov 19, 2010
OSTEON, OSTEON SINUS, OSTEON LIFTING
Dental
126d
Cleared
Oct 09, 2009
RAINBOW BLOCK
Dental
53d
Cleared
Apr 24, 2007
OSTEON, MODELS GBG0305, GBG0510, GBG1020, GBG2030, GBG3040, GBG4050
Dental
215d