Data / Medical devices / United States / MOTUS GI Inc
MOTUS GI Inc: FDA-registered device maker in Fort Lauderdale, FL, United States, 1 510(k) clearance
MOTUS GI Inc is registered with the FDA (registration 3013184907) in Fort Lauderdale, FL, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 10, 2022. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3013184907
- Address
- 1301 E Broward Blvd Suite 310, Fort Lauderdale, FL, United States, 33301
- Owner or operator
- MOTUS GI Medical Technologies Ltd (10053317)
- Roles
- Complaint file establishment
- First device listed
- June 28, 2019
- Registered through
- 2026
- Brand names listed
- Endoscopy Cart, Pure-Vu EVS System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Colonoscope And Accessories, Flexible/Rigid | FDF | 2 | Complaint file establishment | accessdata.fda.gov |
| Stand, Infusion | FOX | 1 | Complaint file establishment | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 10, 2022 | K220007 | Pure-Vu EVS System | FDF | Substantially Equivalent | Motus GI Medical Technologies , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated February 10, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.