Cry IQ AB
SwedenFDA 510(k) applicant, unverified
- Devices
- 1
What Cry IQ AB makes
Cry IQ AB manufactures cryotherapy devices, including the CryoIQ DERM for dermatological applications, the CryoIQ PRO for general medical use, and the CryoIQ EquiMED for veterinary treatments. These devices use controlled cryotherapy to deliver precise freezing treatments for skin conditions, tissue ablation, and equine therapy.
The company’s portfolio consists of Class II medical devices, which are regulated under the FDA’s 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) database and are intended for use in the United States. The manufacturer is based in the US.
Catalogue
CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED Ref K172049
510(k) 510(k)
Frequently asked questions
How many devices does Cry IQ AB have in the registry?
The registry currently lists 1 device for Cry IQ AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cry IQ AB's devices?
Among its 1 most recently registered device, Cry IQ AB has devices listed in FDA 510(k) (1 device).
What risk classes do Cry IQ AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cry IQ AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cry IQ AB in the registry?
The most recently registered devices listed for Cry IQ AB include CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED.