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 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Signus Medical, LLC with 8 510(k) clearances. The most recent is a 510(k) clearance dated Sep 18, 2009: DIANA FUSION CAGE.
| Sep 18, 2009 | DIANA FUSION CAGEK091122 · MAX | 510(k) clearances |
| Aug 7, 2009 | MONOPOLY PEDICLE SCREW SYSTEMK092073 · NKB | 510(k) clearances |
| Jul 14, 2008 | MONOPOLY PEDICLE SCREW SYSTEMK081108 · NKB | 510(k) clearances |
| Aug 16, 2005 | NUBIC SPINAL IMPLANTK052096 · MQP | 510(k) clearances |
| Oct 22, 2003 | CONKLUSION PEDICLE SCREW SYSTEMK031455 · MNI | 510(k) clearances |
| Jul 30, 2003 | PEEK TETRIS SPINAL IMPLANTK031757 · MQP | 510(k) clearances |
| Apr 8, 2003 | TETRIS SPINAL IMPLANTK022793 · MQP | 510(k) clearances |
| Jun 11, 2002 | RABEA CEMENT RESTRICTORK020836 · JDK | 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
