Adiatec SA
FranceFDA applicant, unverified
- Devices
- 1
What Adiatec SA makes
Adiatec SA manufactures the LacryTest, a diagnostic device used to assess tear film production and evaluate dry eye conditions by measuring basal tear secretion rates.
The LacryTest is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Lacrytest Ref K034057
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Adiatec SA have in the registry?
The registry currently lists 1 device for Adiatec SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adiatec SA's devices?
Among its 1 most recently registered device, Adiatec SA has devices listed in FDA 510(k) (1 device).
What risk classes do Adiatec SA's devices fall under?
Among its 1 most recently registered device, the classes recorded for Adiatec SA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Adiatec SA in the registry?
The most recently registered devices listed for Adiatec SA include LACRYTEST.