Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Lumisys with 7 510(k) clearances. The most recent is a 510(k) clearance dated May 11, 1998: LUMISCAN 135 PHOSPHOR PLATE DIGITIZER/LUMISYS 135 ERASER.
| May 11, 1998 | LUMISCAN 135 PHOSPHOR PLATE DIGITIZER/LUMISYS 135 ERASERK980809 · LMA | 510(k) clearances |
| Mar 17, 1998 | DI-2000K980213 · LMA | 510(k) clearances |
| Oct 18, 1995 | LUMISYS DICOM TOOKLITK953371 · LMD | 510(k) clearances |
| Sep 18, 1995 | LUMISYS, LUMISCAN 20K953964 · LMA | 510(k) clearances |
| Oct 7, 1993 | LUMISCAN 50K933129 · LMA | 510(k) clearances |
| Mar 4, 1991 | COMPACT LASER IMAGER, MODEL CLI-100K902347 · LMC | 510(k) clearances |
| Apr 30, 1990 | DIGITAL IMAGE SCANNER, MODEL DIS-1000K901423 · LMA | 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
