Data / Medical devices / Spain / Batec Mobility S.L
Batec Mobility S.L: FDA-registered device maker in Sant Quirze Del Valles Barcelona, Spain, 1 510(k) clearance
Batec Mobility S.L is registered with the FDA (registration 3011749761) in Sant Quirze Del Valles Barcelona, Spain. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 7, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011749761
- Address
- Illa De Buda, 2, Sant Quirze Del Valles Barcelona, Spain, E-08192
- Owner or operator
- Batec Mobility S.L (10093061)
- Roles
- Manufacturer
- First device listed
- March 25, 2025
- Registered through
- 2026
- Brand names listed
- MINI2, ELECTRIC 2, RAPID 2, SCRAMBLER 2
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Powered | ITI | 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 |
|---|---|---|---|---|---|---|
| March 7, 2025 | K241159 | Handbike Batec Electric | ITI | Substantially Equivalent | Batec Mobility, S.L. | accessdata.fda.gov |
Compare with other makers
Updated March 7, 2025. 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.