Linatech, LLC
United StatesFDA applicant, unverified FDA FEI 3007037519
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Tigrt Tps Ref K090893
Regimes: 510(k) Registry: 510(k)Tigrt Mlc, Tigrt Dmlc Ref K090802
Regimes: 510(k) Registry: 510(k)Tigrt Ivs Ref K092550
Regimes: 510(k) Registry: 510(k)VenusX Ref K232489
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3007037519
- Address
- 1294 Kifer Road, # 705, Sunnyvale, CA, 94086
Frequently asked questions
How many devices does Linatech, LLC have in the registry?
The registry currently lists 4 devices for Linatech, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Linatech, LLC's devices?
Among its 4 most recently registered devices, Linatech, LLC has devices listed in FDA 510(k) (4 devices).
What risk classes do Linatech, LLC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Linatech, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Linatech, LLC in the registry?
The most recently registered devices listed for Linatech, LLC include TIGRT TPS, TIGRT MLC, TIGRT DMLC, TIGRT IVS and VenusX.