FDA Device Intelligence
Home › Aesculap AG › SQ.LINE

SQ.LINE

Aesculap AG · Model LX157NR · UDI-DI 04046955282722

HXZ Prescription
1
510(k) clearances
513
Adverse events
1
Recalls
247
Facilities

Description

SQ.LINE TC Wire Cutting Forceps, 9 1/2", (240 mm), ergonomic handle, double articulated joint, up to Ø 2.0 mm, non-sterile, reusable

Recalls

DateFirmReason
2020-11-20Zimmer Biomet, Inc.Device has the potential for fracture during use.

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.