FDA Device Establishments · JSON-LD · Markdown

Penumbra Inc.

FEI 3013758550 · Manufacture Medical Device · Status: Active

FEI Number3013758550
Owner / OperatorPENUMBRA, INC. (#9072336)
Address6262 Patterson Pass Rd,, Suite A, Suite E, Suite F, 6336 Patterson Pass Rd, Suite D, Livermore, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)QEW
Regulation § (21 CFR)870.5150
Proprietary namesIndigo Aspiration System – Lightning Aspiration Tubing

External sources

Source: openFDA. Public-domain (CC0).