FDA Device Intelligence
HomeAESCULAP, INC. › AESCULAP

AESCULAP

AESCULAP, INC. · Model MA704R · UDI-DI 04046964589393

JYR Prescription
2
510(k) clearances
6
Adverse events
0
Recalls
70
Facilities

Description

LEMPERT Malleus Nipper, 4 1/2", (115 mm), (11 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 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.