Elliquence, LLC - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Elliquence, LLC has 8 FDA 510(k) cleared medical devices. Based in Shelton, US.
Latest FDA clearance: Jan 2025. Active since 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Elliquence, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Elliquence, LLC
8 devices
Cleared
Jan 24, 2025
AxCess® Expandable Interbody System
Orthopedic
51d
Cleared
Jun 11, 2018
Endiscope, Endiscope Cervical
Orthopedic
80d
Cleared
May 03, 2017
Surgi Max Ultra
General & Plastic Surgery
111d
Cleared
Jan 06, 2017
Disc-FX System
General & Plastic Surgery
121d
Cleared
Mar 07, 2016
Cobbra RF Tissue Dissector
General & Plastic Surgery
59d
Cleared
Oct 30, 2015
Elliquence Electrodes
General & Plastic Surgery
428d
Cleared
Oct 08, 2013
MEDDUSA BIPOLAR SYSTEM
General & Plastic Surgery
265d
Cleared
Aug 25, 2010
SURGIMAX/ SURGIMAX PLUS
General & Plastic Surgery
190d