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AESCULAP

Aesculap AG · Model DA091 · UDI-DI 04038653145706

EAX Prescription
10
510(k) clearances
47
Adverse events
1
Recalls
371
Facilities

Description

Mouth Mirror Handle, 5 1/2" (135 mm), peek handle, plastic, grey

Recalls

DateFirmReason
2021-03-23Sunstar Americas, Inc.Product may be contaminated with Burkholderia contaminans.

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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.