# Umeheal, Ltd.

- Location (FDA's records): Shenzhen, CN
- FDA decisions: 1 (2019–2019): 1 510(k) clearance
- Product codes: IPF (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Jkh Health Co., Ltd.: 1 (https://510kreport.com/company/jkh-health)
- Philips Consumer Lifestyle B.V.: 1 (https://510kreport.com/company/philips-consumer-lifestyle)

## Firms that cite its devices most
- Cymedica Orthopedics, Inc.: 1 (https://510kreport.com/company/cymedica-orthopedics)

## Its most-cited devices
- K192733: RelieforMe TENS/EMS Device Model UPK-GE01 (2019), cited by 1

## Recent decisions
- K192733: RelieforMe TENS/EMS Device Model UPK-GE01 (Dec 23, 2019)

Source page: https://510kreport.com/company/umeheal