Telesis Technologies, Inc.
TaiwanFDA applicant, unverified
- Devices
- 1
What Telesis Technologies, Inc. makes
Telesis Technologies, Inc. manufactures the Telesis Digital Infrared Thermal Image System, Spectrum 9000MB, a device designed for thermal imaging applications.
The Spectrum 9000MB is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Telesis Technologies, Inc. have in the registry?
The registry currently lists 1 device for Telesis Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Telesis Technologies, Inc.'s devices?
Among its 1 most recently registered device, Telesis Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Telesis Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Telesis Technologies, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Telesis Technologies, Inc. in the registry?
The most recently registered devices listed for Telesis Technologies, Inc. include TELESIS DIGITAL INFRARED THERMAL IMAGE SYSTEM, SPECTRUM 9000MB.