FDA Device Intelligence
Home › Aesculap AG › SQ.LINE

SQ.LINE

Aesculap AG · Model KH113NR · UDI-DI 04046955286065

HXL Prescription
3
510(k) clearances
74
Adverse events
1
Recalls
202
Facilities

Description

SLOTTED MALLET 680GR.HEAD

Recalls

DateFirmReason
2021-07-21Implant Resource IncPotential for mallet head to become separated from mallet handle. There is also significant deformations on striking surface that were not expected

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.