Medical Device Manufacturer · US , Shelton , CT

Elliquence, LLC - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2010

Recent clearances: AxCess® Expandable Interbody System, Endiscope, Endiscope Cervical

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
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