Data / Medical devices / Switzerland / Djo Global Switzerland Sarl
Djo Global Switzerland Sarl: FDA-registered device maker in Ecublens Vaud, Switzerland, 1 510(k) clearance
Djo Global Switzerland Sarl is registered with the FDA (registration 3003678958) in Ecublens Vaud, Switzerland. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 17, 2002. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3003678958
- Address
- ZI Larges Pieces A Chemin du Devent, Ecublens Vaud, Switzerland, CH-1024
- Owner or operator
- DJO, LLC (9015378)
- Roles
- Specification developer
- First device listed
- July 6, 2009
- Registered through
- 2026
- Brand names listed
- Compex Fitness Trainer, Compex SP4, Compex Sport, Compex Sport 4
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 |
|---|---|---|---|---|---|---|
| April 17, 2002 | K011880 | COMPEX SPORT | NGX | Substantially Equivalent | Compex S.A. | accessdata.fda.gov |
Compare with other makers
Updated April 17, 2002. 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.