Data / Medical devices / United States / Katalyst Interactive Inc.
Katalyst Interactive Inc.: FDA-registered device maker in Incline Village, NV, United States, 1 510(k) clearance
Katalyst Interactive Inc. is registered with the FDA (registration 3042971880) in Incline Village, NV, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 3, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3042971880
- Address
- 930 Tahoe Blvd STE, Incline Village, NV, United States, 89451
- Owner or operator
- Katalyst Interactive Inc. (10057482)
- Roles
- Specification developer
- First device listed
- August 15, 2020
- Registered through
- 2026
- Brand names listed
- Katalyst Training System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | 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 |
|---|---|---|---|---|---|---|
| February 3, 2020 | K190966 | Katalyst Training System | NGX | Substantially Equivalent | Katalyst, Inc. | accessdata.fda.gov |
Compare with other makers
Updated February 3, 2020. 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.