Data / Medical devices / Spain / Capenergy Medical, S.L.
Capenergy Medical, S.L.: FDA-registered device maker in Sant Joan Despi Barcelona, Spain, 2 510(k) clearances
Capenergy Medical, S.L. is registered with the FDA (registration 3016675013) in Sant Joan Despi Barcelona, Spain. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 28, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016675013
- Address
- Pol. Ind. Fontsanta Av. Mare de deu de Monserrat 41 bis Pje 1 Derecha, Sant Joan Despi Barcelona, Spain, 08970
- Owner or operator
- Capenergy Medical, S.L. (10062766)
- Roles
- Manufacturer
- First device listed
- March 6, 2020
- Registered through
- 2026
- Brand names listed
- C Beauty, C1, C2, C3 and C4, Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500, Capenergy- C 100, C 200, C 300, C 400, C 50
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Vacuum, Radio Frequency Induced Heat | PBX | 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 28, 2023 | K222260 | Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500 | PBX | Substantially Equivalent | Capenergy Medical S.L. | accessdata.fda.gov |
| February 11, 2020 | K191202 | CAPENERGY - C100, C200, C300, C400, C50 | PBX | Substantially Equivalent | Capenergy Medical S.L. | accessdata.fda.gov |
Compare with other makers
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Massager, Vacuum, Radio Frequency Induced Heat
Updated March 28, 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.