Teca, Inc.
United StatesFDA applicant, unverified
- Devices
- 29
What Teca, Inc. makes
Teca, Inc. manufactures diagnostic and monitoring devices for neurological assessments, including electroencephalographs (EEG) like the P460 and DG32, transcranial Doppler systems (e.g., TC2-64), and evoked response stimulators (e.g., #ST10 and LS-05 LED Stimulator). Their portfolio also includes electromyographs (e.g., Model-10 and Model B9), montage systems (e.g., Montage II), and specialized tools like the reversing click generator (RCG6) and neuromapping software (NeuroMapper 386).
The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory submissions recorded in the FDA’s 510(k) database. These products are intended for use in clinical and research settings for neurological diagnostics and are listed under U.S. regulatory authorities. Teca, Inc. is headquartered in the United States.
Catalogue
Search and filter all 29 devicesFrequently asked questions
How many devices does Teca, Inc. have in the registry?
The registry currently lists 29 devices for Teca, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Teca, Inc.'s devices?
Among its 29 most recently registered devices, Teca, Inc. has devices listed in FDA 510(k) (29 devices).
What risk classes do Teca, Inc.'s devices fall under?
Among its 29 most recently registered devices, the classes recorded for Teca, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Teca, Inc. in the registry?
The most recently registered devices listed for Teca, Inc. include P460, DG32 ELECTROENCEPHALOGRAPH, TECA TC2-64 TRANSCRANIAL DOPPLER, REVERSING CLICK GENERATOR RCG6 and #ST10 PROGR. EVOKED RESPONSE STIMULATOR.