Gtg Wellness Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Gtg Wellness Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Opera Lebody (Gold), Opera Lebody (Zafiro)
1
Total
1
Cleared
0
Denied
Gtg Wellness Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Yongin-Si, KR.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Gtg Wellness Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdr Solutions Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Gtg Wellness Co., Ltd.
1 devices