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Medline

MEDLINE INDUSTRIES, INC. · Model WCAA0015 · UDI-DI 10193489019315

IMM
2
510(k) clearances
42
Adverse events
0
Recalls
64
Facilities

Description

FOOTREST SET, K1, K2, K4, WIDES

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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.