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AESCULAP

Aesculap AG · Model FK510R · UDI-DI 04038653166541

HTP Prescription
5
510(k) clearances
9
Adverse events
0
Recalls
78
Facilities

Description

Bone File, 11 3/4" (295 mm), serrated (cross), width: 20 mm

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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.