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AESCULAP

AESCULAP, INC. · Model MA655R · UDI-DI 04046964566356

KBJ Prescription
1
510(k) clearances
2
Adverse events
1
Recalls
77
Facilities

Description

JONES Adenoid Curette, 8 7/8", (225 mm), #2, 6 mm, non-sterile, reusable

Recalls

DateFirmReason
2004-01-29Medtronic Xomed, Inc.The box label indicates that the product is a size 2 whereas a size 4 was packed inside.

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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.