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AESCULAP

AESCULAP, INC. · Model MA567R · UDI-DI 04046964588372

KTF Prescription
0
510(k) clearances
11
Adverse events
0
Recalls
51
Facilities

Description

WILDE ETHMOID FCPS#0 UPTURN 3.5X12 111MM

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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.