# Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd.

- Location (FDA's records): Ljubljana, SI
- FDA decisions: 2 (2018–2020): 2 510(k) clearances
- Product codes: JOM (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 2 (1 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
- Ld Technology, LLC: 1 (https://510kreport.com/company/ld-technology)

## Firms that cite its devices most
- Medeia, Inc.: 1 (https://510kreport.com/company/medeia)

## Its most-cited devices
- K172655: Automated ankle brachial pressure index measuring device (2018), cited by 2

## Recent decisions
- K201046: Automated ankle brachial pressure index measuring device, MESI mTABLET system (Dec 11, 2020)
- K172655: Automated ankle brachial pressure index measuring device (Jan 11, 2018)

Source page: https://510kreport.com/company/mesi-doo-mesi-development-of-medical-devices