Endologix, Inc.
Endologix, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2012, with 2 FDA device recalls on record.
Top product codes for Endologix, Inc.
FDA recalls by Endologix, Inc.
- Z-2263-2020 — Ovation iX Abdominal Stent Graft Systems, REF: TV-AB2080-I, TV-AB2080-J, TV-AB2380-I, TV-AB2380-J, TV-AB2680-I, TV-AB2680-J, TV-AB2980-I, TV-AB2980-J, TV-AB3480-I, TV-AB3480-J
- Z-1436-2013 — Brand Name: AFX" Introducer System, Model Number S17-45. Lot Numbers: 1079840, 1079843, 1079844, 1079845. Product Usage: The AFX Introducer System is intended for use to facilitate the introduction of catheters and other medical devices into the vasculature and to minimize blood loss associated with such introduction.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Endologix, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.