Weero Co. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Weero Co. - FDA 510(k) Cleared Devices
Recent clearances: Apollo Duet (Model : APD-4000)
1
Total
1
Cleared
0
Denied
Weero Co. has 1 FDA 510(k) cleared medical devices. Based in Suwon-Si, KR.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Weero Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Weero Co.
1 devices