Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Elliquence, LLC with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jan 24, 2025: AxCess® Expandable Interbody System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 24, 2025 | AxCess® Expandable Interbody SystemK243739 · MAX | 510(k) clearances |
| Jun 11, 2018 | Endiscope, Endiscope CervicalK180766 · HRX | 510(k) clearances |
| May 3, 2017 | Surgi Max UltraK170107 · GEI | 510(k) clearances |
| Jan 6, 2017 | Disc-FX SystemK162490 · GEI | 510(k) clearances |
| Mar 7, 2016 | Cobbra RF Tissue DissectorK160041 · GEI | 510(k) clearances |
| Oct 30, 2015 | Elliquence ElectrodesK142410 · GEI | 510(k) clearances |
| Oct 8, 2013 | MEDDUSA BIPOLAR SYSTEMK130110 · GEI | 510(k) clearances |
| Aug 25, 2010 | SURGIMAX/ SURGIMAX PLUSK100390 · GEI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
