Home › AESCULAP, INC. › AESCULAP
AESCULAP
AESCULAP, INC. · Model US120 · UDI-DI 04046955077014
EFL
Prescription
5
510(k) clearances
2
Adverse events
0
Recalls
197
Facilities
Description
DE BAKEY TC Tissue Forceps, 9", (230 mm), non-sterile, reusable
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 docsData 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.
