# Penumbra Inc.

FEI: 3016591327
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: PENUMBRA, INC. (#9072336)

Address: 630 Roseville Parkway, Roseville, CA, US



## Products

Total registered: 2
Top product codes: HCG, KRD
Regulation §: 882.5950, 870.3300

Proprietary names: PC 400, Penumbra Coil System, Ruby Coil System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223016591327%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3016591327