FDA Device Intelligence
Home › AESCULAP IMPLANT SYSTEMS, LLC › AESCULAP

AESCULAP

AESCULAP IMPLANT SYSTEMS, LLC · Model ME183R · UDI-DI 04046964816673

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

Description

COBB ELEVATOR ANTERIOR APPROACH (3/4")

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.