Data / Medical devices / Switzerland / Valley Electronics AG
Valley Electronics AG: FDA-registered device maker in Zurich, Switzerland, 1 510(k) clearance
Valley Electronics AG is registered with the FDA (registration 3011197658) in Zurich, Switzerland. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 20, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011197658
- Address
- Wengistrasse 2, Zurich, Switzerland, 8004
- Owner or operator
- Valley Electronics AG (10047398)
- Roles
- Manufacturer, Specification developer
- First device listed
- August 22, 2014
- Registered through
- 2026
- Brand names listed
- Daysy, Daysy USA, Lady-Comp
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Fertility Diagnostic, Proceptive | LHD | U | Manufacturer, 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 20, 2006 | K050094 | LADY COMP USA | LHD | Substantially Equivalent | Lady Comp USA | accessdata.fda.gov |
Compare with other makers
Updated April 20, 2006. 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.