# Motus GI Medical Technologies, Ltd.

- Location (FDA's records): Tirat Carmel, IL
- FDA decisions: 7 (2016–2023): 7 510(k) clearances
- Product codes: FDF (7)
- 510(k) review time since 2016: median 31 days, against 98 for FDA's reviews in the same codes and years (5 of 7 faster)
- Predicates its devices cite: 7 (6 its own); citations of its devices by later devices: 7 (6 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
- Easyglide, Ltd.: 1 (https://510kreport.com/company/easyglide)

## Firms that cite its devices most
- Neptune Medical, Inc.: 1 (https://510kreport.com/company/neptune-medical)

## Its most-cited devices
- K191220: Pure Vu System (2019), cited by 2
- K160015: Pure Vu (2016), cited by 1
- K173392: Pure-Vu System (2017), cited by 1
- K232922: Pure-Vu EVS System (2023), cited by 1
- K181437: Pure Vu System (2018), cited by 1
- K220007: Pure-Vu EVS System (2022), cited by 1

## Recent decisions
- K232922: Pure-Vu EVS System (Oct 20, 2023)
- K220007: Pure-Vu EVS System (Feb 10, 2022)
- K210981: Pure Vu System (Apr 29, 2021)
- K191220: Pure Vu System (Jun 6, 2019)
- K181437: Pure Vu System (Jun 21, 2018)
- K173392: Pure-Vu System (Dec 12, 2017)
- K160015: Pure Vu (Sep 22, 2016)

Source page: https://510kreport.com/company/motus-gi-medical-technologies