FDA Device Intelligence
Home › Omni International Corp. › OmniTrustTM

OmniTrustTM

Omni International Corp. · Model 50325-19 · UDI-DI 50810572000095

HOY
10
510(k) clearances
51
Adverse events
1
Recalls
720
Facilities

Description

Face Shield

Recalls

DateFirmReason
2008-06-05Phillips Safety ProductsRadiation Protective Eyewear does not meet the radiation protection levels stated on the labeling.

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.