Temtech, Ltd.
IrelandFDA applicant, unverified
- Devices
- 1
What Temtech, Ltd. makes
Temtech, Ltd. manufactures the LITEGUARD 9, a device designed for surgical lighting applications in operating rooms, ensuring precise illumination for medical procedures.
The LITEGUARD 9 is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Liteguard 9 Ref K851924
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Temtech, Ltd. have in the registry?
The registry currently lists 1 device for Temtech, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Temtech, Ltd.'s devices?
Among its 1 most recently registered device, Temtech, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Temtech, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Temtech, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Temtech, Ltd. in the registry?
The most recently registered devices listed for Temtech, Ltd. include LITEGUARD 9.