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FOOTREST

Pride Mobility Products Corp · Model FOOTREST · UDI-DI 00606509900041

IMM Prescription
2
510(k) clearances
37
Adverse events
0
Recalls
64
Facilities

Description

A device intended to be used to sustain/retain a patient's foot or feet in a desired position. This device will often be considered an accessory to one or more parent devices.

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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.