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Argus ll Retinal Implant Kit

Second Sight Medical Products, Inc. · Model 011014-002-K · UDI-DI 00856264005301

NBF Prescription
0
510(k) clearances
93
Adverse events
0
Recalls
1
Facilities

Description

The retinal prosthesis implant is responsible for receiving information from the external components of the system and electrically stimulating the retina to induce visual perception.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.