Vistek Corp.
United StatesFDA applicant, unverified
- Devices
- 5
What Vistek Corp. makes
Vistek Corp. manufactures medical video systems, including the VIS-2000 and VIS-1000, designed for endoscopic and surgical imaging applications. Their portfolio also includes the LCA 2000, an imaging control system, and the VISTEK Electronic Controller for procedural monitoring. The company produces high-intensity light sources like the VLS 5300 300W Xenon Light Source for surgical illumination.
The company’s devices are classified under FDA regulations as Class I and Class II, with some models requiring 510(k) clearance. These products are listed in the FDA’s 510(k) registry, reflecting their regulatory status. Vistek Corp. is headquartered in the United States.
Catalogue
Vis-2000 Video System Ref K860173
Regimes: 510(k) Registry: 510(k)Vis-1000 Video System Ref K843806
Regimes: 510(k) Registry: 510(k)Lca 2000 Ref K871034
Regimes: 510(k) Registry: 510(k)Vistek Electronic Controller Ref K904682
Regimes: 510(k) Registry: 510(k)Vls 5300 300W Xenon Light Source Ref K904681
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vistek Corp. have in the registry?
The registry currently lists 5 devices for Vistek Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vistek Corp.'s devices?
Among its 5 most recently registered devices, Vistek Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Vistek Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Vistek Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vistek Corp. in the registry?
The most recently registered devices listed for Vistek Corp. include VIS-2000 VIDEO SYSTEM, VIS-1000 VIDEO SYSTEM, LCA 2000 and VISTEK ELECTRONIC CONTROLLER.