FDA Device Establishments · JSON-LD · Markdown

Penumbra Inc.

FEI 3016591327 · Manufacture Medical Device · Status: Active

FEI Number3016591327
Owner / OperatorPENUMBRA, INC. (#9072336)
Address630 Roseville Parkway, Roseville, CA, US
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)HCG, KRD
Regulation § (21 CFR)882.5950, 870.3300
Proprietary namesPC 400; Penumbra Coil System; Ruby Coil System

External sources

Source: openFDA. Public-domain (CC0).