Renaissance Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Renaissance Technology, Inc. makes
Renaissance Technology, Inc. manufactures the IQ System, a medical device designed for [specific clinical application not detailed in data]. The device is intended for [purpose implied by Class II designation, e.g., diagnostic, monitoring, or therapeutic use in controlled environments].
The IQ System is classified as a Class II device under FDA regulations and requires 510(k) clearance for market authorisation. The company is based in the United States.
Catalogue
Frequently asked questions
How many devices does Renaissance Technology, Inc. have in the registry?
The registry currently lists 2 devices for Renaissance Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Renaissance Technology, Inc.'s devices?
Among its 2 most recently registered devices, Renaissance Technology, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Renaissance Technology, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Renaissance Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Renaissance Technology, Inc. in the registry?
The most recently registered devices listed for Renaissance Technology, Inc. include IQ SYSTEM.