# Toshiba Medical Systems Corporation, Japan

- Location (FDA's records): Tustin, CA
- FDA decisions: 9 (2011–2017): 9 510(k) clearances
- Product codes: LNH (2), JAK (2), MOS (2), IYN (1), ITX (1), JAA (1)
- Predicates its devices cite: 10 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Toshiba America Medical Systems, In.C: 7 (https://510kreport.com/company/toshiba-america-medical-systems-in-c)
- Toshibamedical Systems Corporation: 3 (https://510kreport.com/company/toshibamedical-systems)

## Firms that cite its devices most
- Toshiba America Medical Systems, In.C: 2 (https://510kreport.com/company/toshiba-america-medical-systems-in-c)
- Quality Electrodynamics, LLC: 1 (https://510kreport.com/company/quality-electrodynamics)
- Toshibamedical Systems Corporation: 1 (https://510kreport.com/company/toshibamedical-systems)

## Its most-cited devices
- K102489: Vantage Titan 3T (2011), cited by 2
- K121577: Aplio Artida Diagnostic Ultrasound System (2012), cited by 1
- K103645: Aplio XG Diagnostic Ultrasound System (2011), cited by 1

## Recent decisions
- K172878: Vantage Titan 3T, MRT-3010/A7, M-Power GX (Nov 17, 2017)
- K133324: Suresubtraction Lung (Sep 5, 2014)
- K121911: Octave Speeder Spine (Aug 17, 2012)
- K121910: Octave Speeder Head (Aug 17, 2012)
- K121577: Aplio Artida Diagnostic Ultrasound System (Jun 22, 2012)
- K120546: Aquilion Premium (Jun 13, 2012)
- K112054: Infinix CF-I/SP and Infinix VF-I/SP Model Infx-8000V (Aug 5, 2011)
- K102489: Vantage Titan 3T (Aug 2, 2011)

Source page: https://510kreport.com/company/toshiba-medical-systems-japan