Kinetic Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Kinetic Instruments, Inc. makes
Kinetic Instruments, Inc. manufactures the SunLiteLED Model #2810, a light-based medical device, and the TransCure Model 2910, a transcutaneous energy delivery system. These products are designed for therapeutic or diagnostic applications requiring controlled light or energy transmission through the skin or tissue.
The company’s portfolio consists of Class II devices, each authorised through the FDA’s 510(k) clearance process. These devices are listed under the US regulatory framework, reflecting compliance with applicable medical device standards and requirements.
Catalogue
Sunliteled Model #2810 Ref K012946
Regimes: 510(k) Registry: 510(k)Transcure, Model 2910 Ref K022862
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kinetic Instruments, Inc. have in the registry?
The registry currently lists 2 devices for Kinetic Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kinetic Instruments, Inc.'s devices?
Among its 2 most recently registered devices, Kinetic Instruments, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Kinetic Instruments, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kinetic Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kinetic Instruments, Inc. in the registry?
The most recently registered devices listed for Kinetic Instruments, Inc. include SUNLITELED MODEL #2810 and TRANSCURE, MODEL 2910.