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.
510(k) submissions have been managed by Empirical Technologies as regulatory consultant.
FDA 510(k) Regulatory Record - 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