Data / Medical devices / United States / Vicon Motion Systems Inc
Vicon Motion Systems Inc: FDA-registered device maker in Centennial, CO, United States, 1 510(k) clearance
Vicon Motion Systems Inc is registered with the FDA (registration 1000377231) in Centennial, CO, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 16, 1981. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1000377231
- Address
- 12650 E Arapahoe Rd Suite 200, Centennial, CO, United States, 80112
- Owner or operator
- VICON MOTION SYSTEMS, INC. (1036056)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- June 6, 2013
- Registered through
- 2026
- Brand names listed
- VICON
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Interactive Rehabilitation Exercise Devices | LXJ | 2 | Complaint file establishment, Specification developer | 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 |
|---|---|---|---|---|---|---|
| June 16, 1981 | K811172 | VICON | LXJ | Substantially Equivalent | Oxford Medilog, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 16, 1981. 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.