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EM

Allied Medical, LLC · Model L815000A · UDI-DI 00026072025987

FMR
5
510(k) clearances
126
Adverse events (2 deaths)
0
Recalls
248
Facilities

Description

XTRA BACKBOARD,RED,NO PINS

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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.