Lia Diagnostics
Country not established
Lia Diagnostics is a medical device manufacturer, with 3 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 3
Registry facts
- Registries
- FDA GUDID 2
- FDA 510(k) 1
- Device classes
- FDA Class II 3
What Lia Diagnostics makes
Lia Diagnostics manufactures rapid agglutination test kits for detecting human chorionic gonadotropin beta-subunit (beta-HCG) in clinical settings. These devices are designed for use as in vitro diagnostics to confirm pregnancy through urine samples.
The company’s products are classified as Class II medical devices under FDA regulations and are listed under the 510(k) and UDI programs.
Catalogue
- Registry: GUDID
- Registry: GUDID
LIA Pregnancy Test Ref K171136
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lia Diagnostics have in the registry?
The registry currently lists 3 devices for Lia Diagnostics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lia Diagnostics's devices?
Among its 3 most recently registered devices, Lia Diagnostics has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Lia Diagnostics's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Lia Diagnostics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lia Diagnostics in the registry?
The most recently registered devices listed for Lia Diagnostics include Lia Pregnancy Test 2 Pack Discreet, Lia Pregnancy Test 2 Pack and LIA Pregnancy Test.