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MEDTRONIC XOMED, INC. · Model 0009900 · UDI-DI 20681490013240

EPW Prescription
2
510(k) clearances
2
Adverse events
0
Recalls
9
Facilities

Description

HEADREST 0009900 3PK THORNTON

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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.