Syncro Med Orthopädische Erzeugnisse GmbH
AT-MF-000043210 · Austria · Linz
Syncro Med Orthopädische Erzeugnisse GmbH is registered in the European database on medical devices as a manufacturer, with 314 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 314 |
|---|
Most frequent device types declared: Adju, Drill, Dynamikfuß, H2 Dynamikfuß, Low.
Devices declared under this manufacturer
- Adju Adju Prothesenfuß, 26 cm, links, 2
- Drill Prothesenfuß, links, 24 cm, 1
- Drill Prothesenfuß, links, 26 cm, 1
- Drill Prothesenfuß, rechts, 22 cm, 2
- Drill Prothesenfuß, rechts, 23 cm, 2
- Henrik Dynamikfuß Prothesenfuß, 28 cm, links, 2
- Henrik Dynamikfuß Prothesenfuß, 28 cm, links, 3
- Henrik H2 Dynamikfuß Prothesenfuß, 24 cm, links, 4
- Syncro Dinio Low Prothesenfuß, rechts, 26 cm, 3
- Syncro Dinio Trace Prothesenfuß, links, 22 cm, 1
- Syncro Dinio Trace Prothesenfuß, links, 24 cm, 3
- Syncro Dinio Trace Prothesenfuß, rechts, 25 cm, 2
Showing 12 of 314 declared devices.
Catalogue references include SYPRO-ADJU-26-L-2, SYPRO-DRILL-R-23-2, SYPRO-DYNAM-28-L-2, SYPRO-DYNAM-28-L-3, SYPRO-H2 DY-24-L-4, SYPRO-NORMG-R-24-D.
European nomenclature codes declared: P090699.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 314 |
| Country of registration | Austria |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 314 |
|---|---|
| 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. Syncro Med Orthopädische Erzeugnisse GmbH was not found in either the U.S. or the Canadian register.