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 Arplay Medical with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jul 2, 2002: CRANIAL STEREOTACTIC EQUIPMENT.
| Jul 2, 2002 | CRANIAL STEREOTACTIC EQUIPMENTK010065 · IYE | 510(k) clearances |
| Sep 21, 2001 | INTRA OPERATIVE RADIATION THERAPYK004023 · IYE | 510(k) clearances |
| Jul 12, 2001 | IMMOBILIZATION SYSTEM FOR ENTK003779 · IYE | 510(k) clearances |
| Jun 8, 2001 | BREAST-BOARD (MULTIPLE)K003778 · IYE | 510(k) clearances |
| Apr 18, 2001 | TRAY ADAPTERS, MULTIPLEK010174 · IYE | 510(k) clearances |
| Apr 18, 2001 | LEAD BLOCKSK010172 · IXI | 510(k) clearances |
| Apr 2, 2001 | COUCH FOR TOTAL BODY RADIATIONK010063 · IYE | 510(k) clearances |
| Mar 13, 2001 | STYROFOAM CUTTERS FOR BLOCK CASTING SYSTEMK010062 · IYE | 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
