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Hand Anchor

RIFTON EQUIPMENT · Model K821 · UDI-DI 00858101008407

KID
7
510(k) clearances
12
Adverse events (7 deaths)
0
Recalls
42
Facilities

Description

Arm Anchor

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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.