Company ยท IL
Motus GI Medical Technologies , Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2016 to 2023. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| FDF | Colonoscope And Accessories, Flexible/Rigid | 7 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 20, 2023 | K232922 | Pure-Vu EVS System Motus GI Medical Technologies , Ltd., IL | FDF |
| Feb 10, 2022 | K220007 | Pure-Vu EVS System Motus GI Medical Technologies , Ltd., IL | FDF |
| Apr 29, 2021 | K210981 | Pure Vu System Motus GI Medical Technologies , Ltd., IL | FDF |
| Jun 6, 2019 | K191220 | Pure Vu System Motus GI Medical Technologies , Ltd., IL | FDF |
| Jun 21, 2018 | K181437 | Pure Vu System Motus GI Medical Technologies , Ltd., IL | FDF |
| Dec 12, 2017 | K173392 | Pure-Vu System Motus GI Medical Technologies , Ltd., IL | FDF |
| Sep 22, 2016 | K160015 | Pure Vu Motus GI Medical Technologies , Ltd., IL | FDF |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||