Medical Device Manufacturer · CN , Shenzhen

Umeheal , Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2019

Recent clearances: RelieforMe TENS/EMS Device Model UPK-GE01

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Umeheal , Ltd. Physical Medicine ✕

1 devices

1-1 of 1

Cleared Dec 23, 2019

RelieforMe TENS/EMS Device Model UPK-GE01

Physical Medicine · 87d

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Jun 03, 2026