FDA Device Intelligence
Home › ORMCO CORPORATION › Optiview

Optiview

ORMCO CORPORATION · Model 716-0050 · UDI-DI 00889989059977

EIG Prescription
8
510(k) clearances
34
Adverse events
0
Recalls
337
Facilities

Description

OPTIVIEW STD UNIV LIP and CHEEK RETRACTOR - 2PK

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.