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TIDI

TIDI PRODUCTS, LLC · Model 1027 · UDI-DI 00618125169641

KNP

510(k) clearances

120

Adverse events

Recalls

207

Facilities

Description

TIDI Foot and Ankle Spaceboots Various Various 5.63in x 11.94in x 18.19in 1 per Each

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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.