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OmniTrustTM

OMNI INTERNATIONAL CORP. · Model 212-23 · UDI-DI 00810572001196

OPJ
0
510(k) clearances
22
Adverse events
0
Recalls
152
Facilities

Description

Nitrile Examination Glove Powder Free Large

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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.