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NitriDerm® Ultra Orange™

INNOVATIVE HEALTHCARE CORPORATION · Model 199200 · UDI-DI 20813172020479

QDO LZA LZC

510(k) clearances

Adverse events

Recalls

169

Facilities

Description

Gloves, Exam, Nitrile, Non-Sterile,Powder-Free, Textured, Orange, M

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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.