Lone Star Technologies
Country not established
- Devices
- 2
What Lone Star Technologies makes
Lone Star Technologies manufactures medical devices for creating and managing tissue impressions, including the FLARE, FILE, and FILL systems, as well as the Lone Star Impression Systems. These tools are designed for use in surgical and procedural settings to prepare and shape tissue surfaces.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions recorded in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Flare, File, Fill Ref K981234
Regimes: 510(k) Registry: 510(k)Lone Star Impression Systems Ref K980968
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lone Star Technologies have in the registry?
The registry currently lists 2 devices for Lone Star Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lone Star Technologies's devices?
Among its 2 most recently registered devices, Lone Star Technologies has devices listed in FDA 510(k) (2 devices).
What risk classes do Lone Star Technologies's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lone Star Technologies's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lone Star Technologies in the registry?
The most recently registered devices listed for Lone Star Technologies include FLARE, FILE, FILL and LONE STAR IMPRESSION SYSTEMS.