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IQ

Aesculap AG · Model NS368R · UDI-DI 04046963740351

FZO Prescription
2
510(k) clearances
315
Adverse events
1
Recalls
244
Facilities

Description

IQ FEMUR BOX CHISEL

Recalls

DateFirmReason
2015-06-24Synthes (USA) Products LLCIt was discovered that a 10mm Chisel Blade was etched as a 16mm Chisel Blade.

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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.