Medical device makerLabelled 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 15, 2026, FDA's public records list Intelligent Implant Systems, LLC with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 16, 2018: Mediant Anterior Cervical Plating 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.
| Apr 16, 2018 | Mediant Anterior Cervical Plating SystemK173935 · KWQ | 510(k) clearances |
| Feb 24, 2017 | Revolution™ Spinal Fixation SystemK163056 · NKB | 510(k) clearances |
| Apr 22, 2016 | Revolution Spinal Fixation SystemK160216 · NKB | 510(k) clearances |
| Jan 13, 2015 | Revolution Spinal Fixation SystemK142939 · NKB | 510(k) clearances |
| Oct 25, 2013 | MARAUDER CERVICAL-THORACIC SPINAL FIXATION SYSTEMK132900 · KWP | 510(k) clearances |
| Oct 4, 2012 | ACTIVE SCREW BONE SCREWK121682 · HWC | 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
