Home › AESCULAP, INC. › AESCULAP
AESCULAP
AESCULAP, INC. · Model MA341R · UDI-DI 04046964586415
10
510(k) clearances
482
Adverse events (1 deaths)
2
Recalls
64
Facilities
Description
TAKAHASHI Nasal Forceps, 9 1/2" (210 mm), width: 4 mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-10-30 | Folsom Metal Products, Inc. | Units were not intended for commercial distribution and inadvertently distributed. |
| 2023-10-30 | Folsom Metal Products, Inc. | Units were not intended for commercial distribution and inadvertently distributed. |
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.
