FDA 510(k) Applications Submitted by GENOSS Co., Ltd.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K231480 |
05/22/2023 |
Bright MTA Sealer Plus |
Genoss Co., Ltd. |
| K102015 |
07/16/2010 |
OSTEON, OSTEON SINUS, OSTEON LIFTING |
GENOSS CO., LTD. |
| K102307 |
08/16/2010 |
GENOSS COLLAGEN MEMBRANE MODEL GCM1020, GCM3040 TOTAL 6 MODELS |
GENOSS CO., LTD. |
| K092513 |
08/17/2009 |
RAINBOW BLOCK |
GENOSS CO., LTD. |
| K153676 |
12/21/2015 |
OSTEON III |
GENOSS CO., LTD. |
| K160144 |
01/21/2016 |
rainbow LS Block |
GENOSS CO., LTD. |
| K200153 |
01/22/2020 |
Bright Bond Universal |
GENOSS Co., Ltd. |
| K200155 |
01/22/2020 |
Bright High Flow |
GENOSS Co., Ltd. |
| K062834 |
09/21/2006 |
OSTEON, MODELS GBG0305, GBG0510, GBG1020, GBG2030, GBG3040, GBG4050 |
GENOSS CO., LTD. |
| K112716 |
09/19/2011 |
OSTEON II |
GENOSS CO., LTD. |
| K214086 |
12/27/2021 |
Bright Impress-Light, Bright Impress-Medium, Bright Impress-Heavy, Bright Impress-Bite, Bright Impress-Putty |
Genoss Co., Ltd. |
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