Cortigent, INC.

FDA Device Registration & Listing · Valencia, CA, US · Registration 3004081696

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004081696
FEI Number
3004081696
Entity Name
Cortigent, INC.
City/State/Country
Valencia, CA, US
Establishment Address
27200 Tourney Road, Ste 315, Valencia, CA 91355, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Cortigent, Inc (Owner Number: 10044164)
Owner / Operator Contact Address
27200 Tourney Road, Ste 315, Valencia, CA 91355, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
H110002

All Registered Proprietary Names

Argus II Retinal Prosthesis

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NBF Prosthesis, Retinal Unknown Class f N/A 2013-05-08

Official Correspondent

Uday Patel

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cortigent, Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004081696. Last updated year: 2026. Please use registration number 3004081696 when referencing this establishment in official correspondence.
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