FDA Device Intelligence
HomeAESCULAP, INC. › AESCULAP

AESCULAP

AESCULAP, INC. · Model MA701R · UDI-DI 04046964589379

KAE Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
224
Facilities

Description

Nasal Forceps, straight, 7 1/4", (185 mm), working length: 4 3/4", (120 mm), #1, width: 4,500 mm, stainless steel, non-sterile, reusable

Recalls

DateFirmReason
2025-01-31Aesculap IncThe forceps have been used in ways not covered by the design resulting in breakage of the clamps.

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.