Data / Medical devices / Switzerland / Pixmeo Sarl
Pixmeo Sarl: FDA-registered device maker in Bernex Geneve, Switzerland, 1 510(k) clearance
Pixmeo Sarl is registered with the FDA (registration 3012516536) in Bernex Geneve, Switzerland. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 20, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012516536
- Address
- Pixmeo SARL 266 rue de Bernex, Bernex Geneve, Switzerland, 1233
- Owner or operator
- Pixmeo SARL (10051125)
- Roles
- Manufacturer
- First device listed
- February 5, 2016
- Registered through
- 2026
- Brand names listed
- OsiriX MD
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 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 |
|---|---|---|---|---|---|---|
| August 20, 2010 | K101342 | OSIRIX MD | LLZ | Substantially Equivalent | Pixmeo Sarl | accessdata.fda.gov |
Compare with other makers
Updated August 20, 2010. 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.