Gni Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Gni Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: VENUS Bracket, ROSE Bracket, Orthodontic Fixation Screw [Smart Anchor Miniscrew], ROSA Bracket
3
Total
3
Cleared
0
Denied
Gni Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Hwaseong, KR.
Last cleared in 2021. Active since 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Gni Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by E&M Consulting and E & M.
FDA 510(k) Regulatory Record - Gni Co., Ltd.
3 devices