Ultrast, Inc.
Country not established
- Devices
- 1
What Ultrast, Inc. makes
Ultrast, Inc. manufactures Ultrast Gel, a medical-grade gel designed for wound care or skin preparation applications.
The company’s portfolio is regulated under FDA’s Class II device classification, with products listed via the 510(k) pathway. Ultrast, Inc. is headquartered in the United States.
Catalogue
Ultrast Gel Ref K211691
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultrast, Inc. have in the registry?
The registry currently lists 1 device for Ultrast, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultrast, Inc.'s devices?
Among its 1 most recently registered device, Ultrast, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ultrast, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ultrast, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultrast, Inc. in the registry?
The most recently registered devices listed for Ultrast, Inc. include Ultrast Gel.