Home › AESCULAP, INC. › AESCULAP
AESCULAP
AESCULAP, INC. · Model MA147R · UDI-DI 04046964583957
KAD
Prescription
5
510(k) clearances
21
Adverse events
1
Recalls
120
Facilities
Description
LEMPERT Elevator, curved, 7 1/4", (185 mm), width: 7 mm, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
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.