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OMNI(R) Surgical System (US)

Sight Sciences, Inc. · Model FG 06721 · UDI-DI 00858027006372

HMZMRH Prescription
0
510(k) clearances
28
Adverse events
1
Recalls
34
Facilities

Description

OMNI System for US in a single pack

Recalls

DateFirmReason
2025-09-06Iantrek Inc.Potential for compromised integrity of the sterile packaging.

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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.