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Spud

KATENA PRODUCTS, INC. · Model K2-4000 · UDI-DI 00841668101209

HNA Prescription
2
510(k) clearances
1
Adverse events
0
Recalls
91
Facilities

Description

GOLF CLUB FOREIGN BODY SPUD

Query this across every FDA database — by API.

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.