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Willowwood Global LLC · Model ONE-TFVS-XL-D · UDI-DI 00194711301201

ISPIPMISS Prescription
1
510(k) clearances
11
Adverse events (2 deaths)
1
Recalls
16
Facilities

Description

One TF System, LimbLogic Side, Alpha Duo, Extra Large

Recalls

DateFirmReason
2009-06-23Ossur Engineering, IncThe plastic caps have come off or become loose when the user stepped into their prosthesis.

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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.