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 Orthion Corp. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Oct 14, 1983: MARK V HIGH VOLTAGE GALVANIC STIMULATORR.
| Oct 14, 1983 | MARK V HIGH VOLTAGE GALVANIC STIMULATORRK832546 · IPF | 510(k) clearances |
| Nov 5, 1982 | SHOWER STOOL W/HANDLESK823154 · IKX | 510(k) clearances |
| Nov 5, 1982 | LAVATORY SEAT HEIGHTENERK823155 · ILS | 510(k) clearances |
| Nov 5, 1982 | SESAM TREATMENT TABLEK823150 · INQ | 510(k) clearances |
| Nov 5, 1982 | COLLAPSABLE LAVATORY HEIGHTENERK823156 · ILS | 510(k) clearances |
| Nov 5, 1982 | BATH TUB SEAT & BATH BOARDK823153 · IKX | 510(k) clearances |
| Nov 5, 1982 | OB TRIPP TRANSPORT CHAIRK823151 · INM | 510(k) clearances |
| Nov 5, 1982 | OB TILT TABLEK823149 · INW | 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
