Thiebaud SAS
Country not established FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Thiebaud SAS makes
Thiebaud Sas manufactures the ST'RIM device.
The ST'RIM device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
St'rim Ref K142073
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Thiebaud SAS Paris Ile-de-France · FR FEI 3006798004
Frequently asked questions
How many devices does Thiebaud Sas have in the registry?
The registry currently lists 1 device for Thiebaud Sas. Devices recorded under merged duplicate company entries are counted once.
Which registries list Thiebaud Sas's devices?
Among its 1 most recently registered device, Thiebaud Sas has devices listed in FDA 510(k) (1 device).
What risk classes do Thiebaud Sas's devices fall under?
Among its 1 most recently registered device, the classes recorded for Thiebaud Sas's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Thiebaud Sas in the registry?
The most recently registered devices listed for Thiebaud Sas include ST'RIM.
Which FDA establishments are linked to Thiebaud Sas?
1 FDA establishment is linked to Thiebaud Sas in the registry; they are listed on the company page.