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 Kaycor International with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jan 27, 1997: PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNIT.
| Jan 27, 1997 | PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNITK965072 · EHD | 510(k) clearances |
| Sep 20, 1993 | YOSHIDA/KAYCOR X-707 WALL MOUNTED DENTAL X-RAYK931717 · EAP | 510(k) clearances |
| Aug 26, 1983 | ROBIN CORDLESS HANDPIECEK832063 · EKX | 510(k) clearances |
| Sep 28, 1982 | K30000 DENTAL CHAIRK822740 · KLC | 510(k) clearances |
| Jan 7, 1982 | YOSHIDA RIDO-F, MODEL LM-01K813348 · EKX | 510(k) clearances |
| Aug 24, 1981 | YOSHIDA-PANOURA 10K811210 · | 510(k) clearances |
| Jun 16, 1981 | YOSHIDA AP 100K811211 · EGY | 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
