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 14, 2026, FDA's public records list Ruggles Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Feb 21, 1991: TITANIUM MESH.
| Feb 21, 1991 | TITANIUM MESHK903485 · GWO | 510(k) clearances |
| Sep 20, 1990 | MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENTK902818 · HBG | 510(k) clearances |
| Aug 9, 1990 | LAMINECTOMY ROGEURK902819 · LXH | 510(k) clearances |
| Jul 18, 1990 | ZEPPELIN INSTRUMENTSK902850 · HAO | 510(k) clearances |
| Jun 7, 1989 | TRANS-ORAL DEPTH GAUGEK893415 · LYQ | 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
