# M&T S.R.L.

- Location (FDA's records): Rimini, IT
- FDA decisions: 4 (2017–2024): 4 510(k) clearances
- Product codes: GEX (4)
- 510(k) review time since 2016: median 144 days, against 90 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 12 (2 its own); citations of its devices by later devices: 5 (2 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
- Quanta System Spa: 3 (https://510kreport.com/company/quanta-system)
- Sharplight Technologies, Ltd.: 2 (https://510kreport.com/company/sharplight-technologies)
- Ellipse A/S: 2 (https://510kreport.com/company/ellipse-a-s)
- Palomar Medical Technologies, Inc.: 1 (https://510kreport.com/company/palomar-medical-technologies)
- Alma Lasers, Inc.: 1 (https://510kreport.com/company/alma-lasers)
- Lumenis, Inc.: 1 (https://510kreport.com/company/lumenis)

## Firms that cite its devices most
- I.T.S. Group S.R.L.: 1 (https://510kreport.com/company/its-group)
- Shanghai Bele Medical Technology Co.,Ltd: 1 (https://510kreport.com/company/shanghai-bele-medical-technology)
- Shanghai Apolo Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/shanghai-apolo-medical-technology)

## Its most-cited devices
- K172413: MT ONE (2017), cited by 2
- K192856: MT One (2020), cited by 2
- K191942: MT One Diamond (2019), cited by 1

## Recent decisions
- K240604: Mtone Evo (Mtone Evo) (Sep 20, 2024)
- K192856: MT One (Apr 24, 2020)
- K191942: MT One Diamond (Oct 17, 2019)
- K172413: MT ONE (Oct 6, 2017)

Source page: https://510kreport.com/company/m-t