# Kyocera Medical Technologies Inc. (KMTI)

- Location (FDA's records): Redlands, CA
- FDA decisions: 3 (2023–2026): 3 510(k) clearances
- Product codes: KWQ (2), NKB (1)
- 510(k) review time since 2016: median 51 days, against 64 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 9 (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 whose devices it cites most
- Kyocera Medical Technologies, Inc.: 2 (https://510kreport.com/company/kyocera-medical-technologies)
- Zavation Medical Products, LLC: 1 (https://510kreport.com/company/zavation-medical-products)
- Alliance Partners, LLC: 1 (https://510kreport.com/company/alliance-partners)
- Spinal USA: 1 (https://510kreport.com/company/spinal-usa)
- Renovis Surgical Technologies, LLC: 1 (https://510kreport.com/company/renovis-surgical-technologies)
- Corelink, LLC: 1 (https://510kreport.com/company/corelink)
- Safe Orthopaedics: 1 (https://510kreport.com/company/safe-orthopaedics)
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)

## Firms that cite its devices most
- Kyocera Medical Technologies, Inc.: 1 (https://510kreport.com/company/kyocera-medical-technologies)
- Zsfab, Inc.: 1 (https://510kreport.com/company/zsfab)

## Its most-cited devices
- K231766: Skyway Anterior Cervical Plate System (2023), cited by 1
- K250486: Skyway Anterior Cervical Plate System (2025), cited by 1

## Recent decisions
- K260989: Varion Thoracolumbar Fixation System (May 15, 2026)
- K250486: Skyway Anterior Cervical Plate System (Apr 10, 2025)
- K231766: Skyway Anterior Cervical Plate System (Sep 12, 2023)

Source page: https://510kreport.com/company/kyocera-medical-technologies-kmti