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Elliquence, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243739AxCess® Expandable Interbody SystemJanuary 24, 2025
K180766Endiscope, Endiscope CervicalJune 11, 2018
K170107Surgi Max UltraMay 3, 2017
K162490Disc-FX SystemJanuary 6, 2017
K160041Cobbra RF Tissue DissectorMarch 7, 2016
K142410Elliquence ElectrodesOctober 30, 2015
K130110MEDDUSA BIPOLAR SYSTEMOctober 8, 2013
K100390SURGIMAX/ SURGIMAX PLUSAugust 25, 2010