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AESCULAP

AESCULAP, INC. · Model MB982R · UDI-DI 04046964589690

KAK Prescription
1
510(k) clearances
7
Adverse events
1
Recalls
92
Facilities

Description

FRONTAL OSTIUM SEEKER CVD, RT ANG 210MM

Recalls

DateFirmReason
2012-08-17Vital Signs Colorado Inc.There is a potential for epistaxis during use of the Disposable General Purpose 9 French Temperature Probe.

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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.