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Lac. Dilator

KATENA PRODUCTS, INC. · Model 08-09130 · UDI-DI 00852979003281

HNW Prescription
3
510(k) clearances
50
Adverse events
0
Recalls
139
Facilities

Description

Sisler Punctum Dilator

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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.