La Jolla Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What La Jolla Technology, Inc. makes
La Jolla Technology, Inc. manufactures disposable and reusable self-adhering electrodes for transcutaneous electrical nerve stimulation (TENS), including the DYNEX series. Their portfolio also includes ECG interference filters, such as the TF-03, and dedicated TENS devices like the DYNEX III and NYNEX II.
These products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Dynex Disposable Self-Adhering Electrode W/Tens Ref K870160
Regimes: 510(k) Registry: 510(k)Dynex Reusable, Self-Adhering Electrode W/Tens Ref K854204
Regimes: 510(k) Registry: 510(k)Ecg Interference Filter Tf-03 Ref K832888
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Nynex Ii Ref K830932
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does La Jolla Technology, Inc. have in the registry?
The registry currently lists 5 devices for La Jolla Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list La Jolla Technology, Inc.'s devices?
Among its 5 most recently registered devices, La Jolla Technology, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do La Jolla Technology, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for La Jolla Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from La Jolla Technology, Inc. in the registry?
The most recently registered devices listed for La Jolla Technology, Inc. include DYNEX DISPOSABLE SELF-ADHERING ELECTRODE W/TENS, DYNEX REUSABLE, SELF-ADHERING ELECTRODE W/TENS, ECG INTERFERENCE FILTER TF-03 and DYNEX III TRANSCUTANEOUS ELECTRICAL NERVE STIMULA..