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Ophthalmic Spatula

KATENA PRODUCTS, INC. · Model K3-2341 · UDI-DI 00841668102480

HND Prescription
6
510(k) clearances
90
Adverse events
0
Recalls
161
Facilities

Description

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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.