DBC Global Oy
FI-MF-000024338 · Finland · Espoo
DBC Global Oy is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 12 |
|---|
Most frequent device types declared: DBC C3R 5220, DBC GHR 5420, DBC LTE 6110, DBC LTF 6130, DBC LTL6150.
Among these devices, 1 are declared with a measuring function.
Devices declared under this manufacturer
- DBC C3R Cervical 3D Rotation
- DBC CE Cervical Extension
- DBC GHR Glenohumeral Rotation
- DBC Health
- DBC LTE Lumbar Thoracic Extension
- DBC LTL Lumbar Thoracic Lateral Flexion
- DBC LTR Lumbar Thoracic Rotation
- DBC MB Multipirpose Bench
- DBC MLP Multipurpose Leg Press
- DBC MLU Multipurpose Low-Friction Unit
- DBC SBA Shoulder Blade Adduction
Catalogue references include 6429810980991, DBC GHR 5420, DBC LTL6150, DBC MB 5620, DBC MLP 5610, DBC MLU 5250.
European nomenclature codes declared: Z120602, V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 12 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. DBC Global Oy was not found in either the U.S. or the Canadian register.