Home › TIDI PRODUCTS, LLC › TIDI

TIDI

TIDI PRODUCTS, LLC · Model 1023 · UDI-DI 00618125169634

KNP

510(k) clearances

121

Adverse events

Recalls

210

Facilities

Description

TIDI Foot and Ankle Spaceboots Various Various 5.63in x 10.69in x 16.19in 1 per Each

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

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.