Nordicicemedical AS
Country not established
- Devices
- 1
What Nordicicemedical AS makes
Nordicicemedical AS develops NICE Software, Version 2.1, a digital tool designed for image control and evaluation in medical imaging workflows. The software is intended to assist in processing and analyzing radiographic images, improving diagnostic accuracy and efficiency for healthcare providers.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device. The software is listed in the FDA’s 510(k) database, adhering to U.S. regulatory standards. Nordicicemedical AS is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nordicicemedical AS have in the registry?
The registry currently lists 1 device for Nordicicemedical AS. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nordicicemedical AS's devices?
Among its 1 most recently registered device, Nordicicemedical AS has devices listed in FDA 510(k) (1 device).
What risk classes do Nordicicemedical AS's devices fall under?
Among its 1 most recently registered device, the classes recorded for Nordicicemedical AS's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nordicicemedical AS in the registry?
The most recently registered devices listed for Nordicicemedical AS include NORDIC IMAGE CONTROL AND EVALUATION (NICE) SOFTWARE, VERSION 2.1.