Ltbio Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Ltbio Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: OLIZ LTB-1000A
1
Total
1
Cleared
0
Denied
Ltbio Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Seongnam-Si, KR.
Last cleared in 2022. Active since 2022. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Ltbio Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by KMC, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ltbio Co., Ltd.
1 devices