Technicuff Corp.
United Statesfrom the FDA registration address FDA FEI 1000222013
Technicuff Corp. is a medical device manufacturer, with 29 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 29
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 28
- FDA 510(k) 1
- Device classes
- FDA Class II 29
- Identifiers
- FDA FEI 1000222013
- DUNS 148745805
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 29 devicesCompany details
- FDA FEI number
- 1000222013
- DUNS number
- 148745805
- Address
- 2525 Industrial St., LEESBURG, FL, 34748
Frequently asked questions
How many devices does Technicuff Corp. have in the registry?
The registry currently lists 29 devices for Technicuff Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Technicuff Corp.'s devices?
Among its 29 most recently registered devices, Technicuff Corp. has devices listed in FDA 510(k) (1 device) and FDA GUDID (28 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Technicuff Corp.'s devices fall under?
Among its 29 most recently registered devices, the classes recorded for Technicuff Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Technicuff Corp. in the registry?
The most recently registered devices listed for Technicuff Corp. include Technicuff UT-3962L, Technicuff UP-0925, Technicuff UA-1745L and Technicuff UN-0309.