FDA Device Intelligence
Home › AESCULAP, INC. › AESCULAP

AESCULAP

AESCULAP, INC. · Model MA418R · UDI-DI 04046964587047

KBA Prescription
0
510(k) clearances
1
Adverse events
0
Recalls
86
Facilities

Description

FOMON Bone File, 8 3/8" (215 mm), double ended, toothed (fine coarse), width: 6,50 mm

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.