Data / Medical devices / Spain / Wiemspro S.L
Wiemspro S.L: FDA-registered device maker in Malaga, Spain, 1 510(k) clearance
Wiemspro S.L is registered with the FDA (registration 3015781781) in Malaga, Spain. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 12, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015781781
- Address
- Jacinto Verdaguer, 11, Malaga, Spain, 29002
- Owner or operator
- Wiemspro S.L (10061109)
- Roles
- Exporter to the US
- First device listed
- August 22, 2019
- Registered through
- 2026
- Brand names listed
- Wiemspro
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Exporter to the US | 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 12, 2019 | K181955 | WiEMSpro | NGX | Substantially Equivalent | Medical Cables S.L. | accessdata.fda.gov |
Compare with other makers
Updated February 12, 2019. 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.