Incredivision, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Incredivision, Inc. makes
Incredivision, Inc. manufactures light sources designed for medical procedures, including a xenon-based illumination device and a liquid-based light system rated at 500 watts. These products are intended for surgical and procedural applications requiring precise, high-intensity lighting.
The company’s portfolio is classified under FDA’s Class II regulatory category and is authorised through the 510(k) clearance process. These devices are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.
Catalogue
Xenon Light Source Ref K940963
Regimes: 510(k) Registry: 510(k)Liquid Light 500 Ref K940962
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Incredivision, Inc. have in the registry?
The registry currently lists 2 devices for Incredivision, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Incredivision, Inc.'s devices?
Among its 2 most recently registered devices, Incredivision, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Incredivision, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Incredivision, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Incredivision, Inc. in the registry?
The most recently registered devices listed for Incredivision, Inc. include XENON LIGHT SOURCE and LIQUID LIGHT 500.