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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 IIb2 323

Most frequent device types declared: Cervical Fusion Cage, Size: 14x17x08 mm, Angulation: 06° , Anatomic, Anterior Fusion Cage, Size: 22x29x11 mm, Angulation: 07° , Small, Anterior Fusion Cage, Size: 28x39x10 mm, Angulation: 07° , Large, Cervical Fusion Cage, Size: 16x19x05 mm, Angulation: 02° , Anatomic, Anterior Fusion Cage, Size: 28x44x11 mm, Angulation: 11° , Xlarge.

Among these devices, 2 323 are declared sterile, 2 323 implantable.

No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED2 323
Country of registrationCzechia
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.

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