Uniweb
Country not established FDA
Part of UniWeb BV
Uniweb is a medical device manufacturer, with 1 device listed in FDA GUDID (FDA Class II) as of 15 Nov 2026.
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 1
- Device classes
- FDA Class II 1
- Sites and related companies
- Identifiers
- DUNS 371443982
At a glance
Market reach
- United States
- FDA establishment
What Uniweb makes
Uniweb manufactures electronic hand dynamometers and pinchmeters, devices used to measure grip strength and pinch force for clinical and rehabilitation assessments. The Eforto is a key product in this category, designed to quantify muscle function in patients.
The company’s devices fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. Uniweb operates from the United States, where these products are authorised for commercial distribution.
Catalogue
- Registry: GUDID
Company details
- DUNS number
- 371443982
FDA establishments
- UniWeb BV Meise Vlaams Brabant · BE FEI 3036833417
Frequently asked questions
How many devices does Uniweb have in the registry?
The registry currently lists 1 device for Uniweb. Devices recorded under merged duplicate company entries are counted once.
Which registries list Uniweb's devices?
Among its 1 most recently registered device, Uniweb has devices listed in FDA GUDID (1 device).
What risk classes do Uniweb's devices fall under?
Among its 1 most recently registered device, the classes recorded for Uniweb's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Uniweb in the registry?
The most recently registered devices listed for Uniweb include Eforto M1 Vigorimeter.
Which FDA establishments are linked to Uniweb?
1 FDA establishment is linked to Uniweb in the registry; they are listed on the company page.