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Argus ll Retinal Implant Kit 011014-002-K

by Second Sight Medical Products, Inc.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00856264005301 UDI-DI Date6 May 2015ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Argus ll Retinal Implant Kit
Generic Name
Video-camera epiretinal prosthesis system orbital implant
Model / Ref / Catalog
011014-002-K, 011014-K
Primary DI / UDI-DI
00856264005301
PMA Number
FDA Product Code
NBF
GMDN Term
Video-camera epiretinal prosthesis system orbital implant
Device Class
Unclassified
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Conditional

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No