Data / Medical devices / Switzerland / Wintecare SA
Wintecare SA: FDA-registered device maker in Chiasso Ticino, Switzerland, 1 510(k) clearance
Wintecare SA is registered with the FDA (registration 3013517192) in Chiasso Ticino, Switzerland. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 29, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013517192
- Address
- Via Motta 10, Chiasso Ticino, Switzerland, 6830
- Owner or operator
- Wintecare SA (10061003)
- Roles
- Manufacturer
- First device listed
- July 26, 2019
- Registered through
- 2026
- Brand names listed
- T~PLUS
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| 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 |
|---|---|---|---|---|---|---|
| January 29, 2019 | K181893 | T-PLUS | PBX | Substantially Equivalent | Wintecare SA | accessdata.fda.gov |
Compare with other makers
Updated January 29, 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.