# Konica Minolta, Inc.

- Location (FDA's records): Hino-Shi, JP
- FDA decisions: 25 (2014–2025): 25 510(k) clearances
- Product codes: MQB (12), LLZ (6), IYN (4), IYO (3)
- 510(k) review time since 2016: median 77 days, against 56 for FDA's reviews in the same codes and years (12 of 19 faster)
- Predicates its devices cite: 34 (20 its own); citations of its devices by later devices: 24 (20 its own)
- Recalls linked to its devices: 7 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Konica Minolta Medical & Graphic, Inc.: 7 (https://510kreport.com/company/konica-minolta-medical-graphic)
- Toshiba America Medical Systems, In.C: 4 (https://510kreport.com/company/toshiba-america-medical-systems-in-c)
- Viztek, LLC: 2 (https://510kreport.com/company/viztek)
- Hitachi Aloka Medical, Ltd.: 1 (https://510kreport.com/company/hitachi-aloka-medical)

## Firms that cite its devices most
- Solutions For Tomorrow AB: 2 (https://510kreport.com/company/solutions-for-tomorrow)
- Mediott, Inc.: 2 (https://510kreport.com/company/mediott)

## Its most-cited devices
- K141271: Aerodr System 2 (2014), cited by 3
- K212685: Konicaminolta DI-X1 (2021), cited by 3
- K162504: SKR 3000 (2016), cited by 2
- K182688: SKR 3000 (2018), cited by 2
- K151465: AeroDR SYSTEM 2 (2015), cited by 2
- K180084: Ultrasound System SONIMAGE MX1 (2018), cited by 1

## Recent decisions
- K250665: SKR 3000 (Jun 17, 2025)
- K241319: SKR 3000 (Nov 21, 2024)
- K240281: Bone Suppression Software (May 31, 2024)
- K230906: Konicaminolta DI-X1 (Apr 25, 2023)
- K223267: SKR 3000 (Nov 17, 2022)
- K220993: Ultrasound System SONIMAGE MX1 (Jun 23, 2022)
- K213908: SKR 3000 (Jan 31, 2022)
- K212685: Konicaminolta DI-X1 (Sep 13, 2021)

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