Data / Medical devices / Spain / Creative Fitness Developments SL
Creative Fitness Developments SL: FDA-registered device maker in Valencia Valencia(Province), Spain, 1 510(k) clearance
Creative Fitness Developments SL is registered with the FDA (registration 3027503912) in Valencia Valencia(Province), Spain. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 6, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3027503912
- Address
- Avenida Alfahuir, 40 Bajo Gnesis EMS, Valencia Valencia(Province), Spain, 46020
- Owner or operator
- Creative Fitness Developments SL (10086089)
- Roles
- Manufacturer
- First device listed
- June 12, 2023
- Registered through
- 2026
- Brand names listed
- Gnesis EMS Plus
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Manufacturer | 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 6, 2023 | K230261 | Gnesis EMS Plus | NGX | Substantially Equivalent | Creative Fitness Developments S.L. | accessdata.fda.gov |
Compare with other makers
Updated June 6, 2023. 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.