Umeheal , Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Umeheal , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: RelieforMe TENS/EMS Device Model UPK-GE01
1
Total
1
Cleared
0
Denied
Umeheal , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Umeheal , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Umeheal , Ltd.
1 devices