Litecure LLC
United StatesFDA applicant, unverified FDA FEI 3026668625
Litecure LLC is a medical device manufacturer, with 37 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 37
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 30
- FDA 510(k) 7
- Device classes
- FDA Class II 37
- Identifiers
- FDA FEI 3026668625
- DUNS 858768943
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 37 devicesCompany details
- FDA FEI number
- 3026668625
- DUNS number
- 858768943
- Address
- 3300 Eagle Parkway, Fort Worth, TX, 76177
- Phone
- 1-877-627-3858
Frequently asked questions
How many devices does LITECURE LLC have in the registry?
The registry currently lists 37 devices for LITECURE LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list LITECURE LLC's devices?
Among its 37 most recently registered devices, LITECURE LLC has devices listed in FDA 510(k) (7 devices) and FDA GUDID (30 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do LITECURE LLC's devices fall under?
Among its 37 most recently registered devices, the classes recorded for LITECURE LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LITECURE LLC in the registry?
The most recently registered devices listed for LITECURE LLC include Empower Delivery System PRD-000477-000-02-L, LightForce EXP LTS-1500P, Empower Delivery System PRD-000424-010-01-L and LightForce EXPi LTS-2500.