E-Teng Technology, Inc.
TaiwanFDA 510(k) applicant, unverified FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What E-Teng Technology, Inc. makes
E-Teng Technology, Inc. manufactures the E-TENG Model EOR 1, a Class II medical device designed for electrophysiological recording or stimulation applications in clinical settings.
The company’s portfolio is regulated under the FDA’s 510(k) pathway, with devices listed in the U.S. regulatory system. The company is headquartered in the United States.
Catalogue
E-Teng Model Eor 1 Ref K122562
510(k) 510(k)
FDA establishments
- E-Teng Technology Inc. New Taipei City · TW FEI 3010585416
Frequently asked questions
How many devices does E-Teng Technology, Inc. have in the registry?
The registry currently lists 1 device for E-Teng Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list E-Teng Technology, Inc.'s devices?
Among its 1 most recently registered device, E-Teng Technology, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do E-Teng Technology, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for E-Teng Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from E-Teng Technology, Inc. in the registry?
The most recently registered devices listed for E-Teng Technology, Inc. include E-TENG MODEL EOR 1.
Which FDA establishments are linked to E-Teng Technology, Inc.?
1 FDA establishment is linked to E-Teng Technology, Inc. in the registry; they are listed on the company page.