Data / Medical devices / Sweden / CryoIQ global AB
CryoIQ global AB: FDA-registered device maker in Onsala Halland, Sweden, 1 510(k) clearance
CryoIQ global AB is registered with the FDA (registration 3012913237) in Onsala Halland, Sweden. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 30, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012913237
- Address
- Apelrodsvagen 1, Onsala Halland, Sweden, 43932
- Owner or operator
- CryoIQ global AB (10056378)
- Roles
- Manufacturer
- First device listed
- December 4, 2017
- Registered through
- 2026
- Brand names listed
- CryoIQ MULTI LINE, CryoIQ Derm, CryoIQ PRO, CryoIQ EquiMed, CryoIQ PRO A
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Unit, Cryosurgical, Accessories | GEH | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 30, 2017 | K172049 | CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED | GEH | Substantially Equivalent | Cry IQ AB | accessdata.fda.gov |
Compare with other makers
Updated August 30, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.