# Konica Corp.

- Location (FDA's records): New York, NY
- FDA decisions: 5 (1992–1999): 5 510(k) clearances
- Product codes: LMC (2), KPR (1), MQB (1), LMA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Konica Minolta Medical & Graphic, Inc.: 2 (https://510kreport.com/company/konica-minolta-medical-graphic)

## Its most-cited devices
- K992586: Konica Laser Imager, Drypro Model 722 (1999), cited by 1
- K980873: Konica Direct Digitizer Regius Model 330 (1998), cited by 1

## Recent decisions
- K992586: Konica Laser Imager, Drypro Model 722 (Oct 29, 1999)
- K990359: Konica Direct Digitizer, Model DD-341 (Aug 17, 1999)
- K980873: Konica Direct Digitizer Regius Model 330 (Jun 19, 1998)
- K920769: Konica LI 10 and 10A Laser Imager (May 6, 1992)
- K920558: Konica Direct Digitizer KD-1000 (Mar 6, 1992)

Source page: https://510kreport.com/company/konica