Syntropiq s.r.o.
CZ-MF-000010050 · Czechia · Prague
Syntropiq s.r.o. is registered in the European database on medical devices as a manufacturer, with 2 323 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 2 323 |
|---|
Most frequent device types declared: Anterior Fusion Cage, Size: 22x29x14 mm, Angulation: 00° , Small, Trab, Anterior Fusion Cage, Size: 28x39x11 mm, Angulation: 14° , Large, Holl, Anterior Fusion Cage, Size: 28x44x16 mm, Angulation: 25° , Xlarge, Tra, Posterior Lumbar Fusion Cage, Size: 10x21x07 mm, Angulation: 08° , Ana, Posterior Transforaminal Fusion Cage, Size: 09x29x12 mm, Angulation: 1.
Among these devices, 2 323 are declared sterile, 2 323 implantable.
Devices declared under this manufacturer
- DynamX System
- Dynamx
Showing 12 of 2 323 declared devices.
Catalogue references include 2220511514, 2620461516, 2620511509, 26S16360816, 2728391411, 4109291212.
European nomenclature codes declared: P09070101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 2 323 |
| Country of registration | Czechia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 2 323 |
|---|---|
| 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. Syntropiq s.r.o. was not found in either the U.S. or the Canadian register.