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N/A

TETRA MEDICAL SUPPLY CORP. · Model 9800Y3 · UDI-DI 00614138122017

KNP

510(k) clearances

120

Adverse events

Recalls

207

Facilities

Description

EFO 3/4 INSOLE F 8-9.5 & M 8-8.5

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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.