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Preemie Hand Splint

Bionix, LLC · Model 21150 · UDI-DI 00714646000538

ILH Prescription
10
510(k) clearances
48
Adverse events
1
Recalls
430
Facilities

Description

Sample, Preemie Hand Splint

Recalls

DateFirmReason
2023-08-18North Coast Medical IncThe thumb strap of the wrist and thumb orthosis may contain latex that is not declared in the product labeling.

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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.