Ultroid, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Ultroid, LLC makes
Ultroid, LLC manufactures the Ultroid Hemorrhoid Management System, including its modifications, which are designed for the treatment of hemorrhoidal conditions. These devices are intended to provide non-surgical interventions for managing symptoms associated with hemorrhoids.
The company’s hemorrhoid management devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States, where Ultroid, LLC is based.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Ultroid Hemorrhoid Management System Ref K023706
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultroid, LLC have in the registry?
The registry currently lists 2 devices for Ultroid, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultroid, LLC's devices?
Among its 2 most recently registered devices, Ultroid, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Ultroid, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ultroid, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultroid, LLC in the registry?
The most recently registered devices listed for Ultroid, LLC include MODIFICATION TO ULTROID HEMORRHOID MANAGEMENT SYSTEM and ULTROID HEMORRHOID MANAGEMENT SYSTEM.