Medical Device Manufacturer · KR , Suwon

Weero Co., Ltd. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2024

Total

Cleared

Denied

Weero Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Suwon, KR.

Latest FDA clearance: Jun 2026. Active since 2024. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Weero Co., Ltd. Filter by specialty or product code using the sidebar.

Weero Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Weero Co., Ltd.

5 devices

1-5 of 5