# Wondfo USA Co., Ltd.

FEI: 3016252795
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Wondfo USA Co., Ltd. (#10028951)

Address: 6720 Cobra Way, San Diego, CA, US



## Products

Total registered: 1
Top product codes: QMN
Regulation §: —

Proprietary names: WELLlife™ COVID-19 / Influenza A&B Test, WELLlife™ COVID-19 / Influenza A&B Home Test

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223016252795%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3016252795