FDA Device Intelligence
Home › AESCULAP, INC. › AESCULAP

AESCULAP

AESCULAP, INC. · Model MD563 · UDI-DI 04046963365554

GEG Prescription
10
510(k) clearances
39
Adverse events
0
Recalls
228
Facilities

Description

BENNETT Bone Lever, curved, 9 1/2" (240 mm), width: 25 mm, 44 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.