SPOT

HEALTHY.IO LTD · Model SPOT.EN.GEN · UDI-DI 17290017272501

FXN Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

The SPOT device is intended to provide healthcare professionals with a tool to document, track, and monitor chronic wounds which will aid in wound care management.

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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.