FDA Device Intelligence
Home › FCI S A S FCI 20 22 › OPHTACATH® 2 mm Bilateral Kit

OPHTACATH® 2 mm Bilateral Kit

FCI S A S FCI 20 22 · Model S1.4122 · UDI-DI 13700773735102

OKS
10
510(k) clearances
95
Adverse events
0
Recalls
19
Facilities

Description

A collection of various ophthalmic surgical instruments and the necessary materials intended to be used to perform an ophthalmic surgical procedure; it is not comprised exclusively of dedicated implantation tools and it does not contain any pharmaceuticals. This is a single-use device.

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.