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Handicare

HANDICARE USA, INC. · Model 8A1420 · UDI-DI 00810045514949

INE
1
510(k) clearances
111
Adverse events (3 deaths)
0
Recalls
18
Facilities

Description

Universal Polyslip with H/S - 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.