FDA Device Intelligence
HomeCardinal Health, Inc. › Kendall

Kendall

Cardinal Health, Inc. · Model 30950300 · UDI-DI 20884527005366

FSD
5
510(k) clearances
66
Adverse events
0
Recalls
108
Facilities

Description

Buttonhole Belt,Pink and Blue Striped

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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.