Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Motus GI Medical Technologies , Ltd. · Predicate Candidate Screening
7 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
31 daysmedian FDA review time
262 days90th percentile
7clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K232922 | Pure-Vu EVS System | Motus GI Medical Technologies , Ltd. | 2023-10-20 | 31 | 0 |
| K220007 | Pure-Vu EVS System | Motus GI Medical Technologies , Ltd. | 2022-02-10 | 37 | 0 |
| K210981 | Pure Vu System | Motus GI Medical Technologies , Ltd. | 2021-04-29 | 28 | 0 |
| K191220 | Pure Vu System | Motus GI Medical Technologies , Ltd. | 2019-06-06 | 30 | 0 |
| K181437 | Pure Vu System | Motus GI Medical Technologies , Ltd. | 2018-06-21 | 20 | 0 |
| K173392 | Pure-Vu System | Motus GI Medical Technologies , Ltd. | 2017-12-12 | 43 | 0 |
| K160015 | Pure Vu | Motus GI Medical Technologies , Ltd. | 2016-09-22 | 262 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda