# Pentax of America, Inc.

FEI: 3008780134
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: HOYA Corporation PENTAX Division (#8030235)

Address: 303 Convention Way Ste 1 Ste 3, Redwood City, CA, US



## Products

Total registered: 1
Top product codes: GEH
Regulation §: 878.4350

Proprietary names: C2 CryoAblation Full 8 Catheter

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223008780134%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3008780134