Celleration
Country not established
- Devices
- 4
What Celleration makes
Celleration makes the Celleration Mist Therapy System, a device designed for wound care that delivers a fine mist to support healing.
The Celleration Mist Therapy System is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Celleration Mist Therapy System 5.1 Ref K050129
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Celleration Mist Therapy System Ref DEN040004
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Celleration have in the registry?
The registry currently lists 4 devices for Celleration. Devices recorded under merged duplicate company entries are counted once.
Which registries list Celleration's devices?
Among its 4 most recently registered devices, Celleration has devices listed in FDA 510(k) (4 devices).
What risk classes do Celleration's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Celleration's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Celleration in the registry?
The most recently registered devices listed for Celleration include CELLERATION MIST THERAPY SYSTEM 5.1, MIST 360 SINGLE USE APPLICATOR KIT, MIST 360 SINGLE USE APPLICATOR KIT, CASE OF 12, ULTRAMIST SYSTEM, ULTRAMIST GENERATOR, ULTRAMIST TREATMENT WAND, ULTRAMIST APPLICATOR and CELLERATION MIST THERAPY SYSTEM.