Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in JapanLabelled 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 Konica Corporation with 5 510(k) clearances. The most recent is a 510(k) clearance dated Oct 29, 1999: KONICA LASER IMAGER, DRYPRO MODEL 722.
| Oct 29, 1999 | KONICA LASER IMAGER, DRYPRO MODEL 722K992586 · LMC | 510(k) clearances |
| Aug 17, 1999 | KONICA DIRECT DIGITIZER, MODEL DD-341K990359 · MQB | 510(k) clearances |
| Jun 19, 1998 | KONICA DIRECT DIGITIZER REGIUS MODEL 330K980873 · LMA | 510(k) clearances |
| May 6, 1992 | KONICA LI 10 AND 10A LASER IMAGERK920769 · LMC | 510(k) clearances |
| Mar 6, 1992 | KONICA DIRECT DIGITIZER KD-1000K920558 · KPR | 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
