Mvitro Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Mvitro Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ORTIV (ORTIV-BL, ORTIV-WH)
1
Total
1
Cleared
0
Denied
Mvitro Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Nov 2024. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Mvitro Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mvitro Co., Ltd.
1 devices