Elliquence, LLC
Elliquence, LLC appears in FDA public data with 0 recalls, 8 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jan 24, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K243739 | AxCess® Expandable Interbody System | Jan 24, 2025 |
| K180766 | Endiscope, Endiscope Cervical | Jun 11, 2018 |
| K170107 | Surgi Max Ultra | May 3, 2017 |
| K162490 | Disc-FX System | Jan 6, 2017 |
| K160041 | Cobbra RF Tissue Dissector | Mar 7, 2016 |
| K142410 | Elliquence Electrodes | Oct 30, 2015 |
| K130110 | MEDDUSA BIPOLAR SYSTEM | Oct 8, 2013 |
| K100390 | SURGIMAX/ SURGIMAX PLUS | Aug 25, 2010 |