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DJO SURGICAL

DJO, LLC · Model 803-05-051 · UDI-DI 00888912092333

FZX
10
510(k) clearances
8,516
Adverse events (4 deaths)
0
Recalls
525
Facilities

Description

TRIAL, LINER 22 X 10 X MP11

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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.