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AED

NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Model 501.51BS · UDI-DI 00848657078221

KAE Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
224
Facilities

Description

AED Bipolar Suction Forceps, 45 Degree Up

Recalls

DateFirmReason
2025-01-31Aesculap IncThe forceps have been used in ways not covered by the design resulting in breakage of the clamps.

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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.