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FlexStep

Liftup A/S · Model FlexStep V2 · UDI-DI 05714420034587

PCE
1
510(k) clearances
12
Adverse events (1 deaths)
0
Recalls
12
Facilities

Description

FlexStep V2, 900, 4+1 step, outdoor

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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.