# WOODWAY USA, INC.

FEI: 3000210901
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: WOODWAY USA, INC. (#9026547)

Address: W234n700 Busse Rd, Vernon, WI, US



## Products

Total registered: 1
Top product codes: IOL
Regulation §: 890.5380

Proprietary names: PPS 43, PPS 70, PPS 55, Continuum, 4Front Med, Boost 2, Pro Med, Pro XL Med

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223000210901%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3000210901