Lineus Medical, LLC
Also registered as Lineus Medical
United StatesFDA applicant, unverified FDA FEI 3019511659
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
SafeBreak® Vascular Ref K231957
Regimes: 510(k) Registry: 510(k)SafeBreak® Vascular Ref K223486
Regimes: 510(k) Registry: 510(k)SafeBreak Vascular Ref K222791
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3019511659
- Address
- 179 North Church Avenue, Fayetteville, AR, 72701
Frequently asked questions
How many devices does Lineus Medical, LLC have in the registry?
The registry currently lists 4 devices for Lineus Medical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lineus Medical, LLC's devices?
Among its 4 most recently registered devices, Lineus Medical, LLC has devices listed in FDA 510(k) (3 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Lineus Medical, LLC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Lineus Medical, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lineus Medical, LLC in the registry?
The most recently registered devices listed for Lineus Medical, LLC include SafeBreak - Vascular, SafeBreak® Vascular and SafeBreak Vascular.