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Cynergy

Country not established

Devices
5

What Cynergy makes

Cynergy manufactures a range of medical devices including the Pacemaker models Pacesetter Model 350, Cynergy Model 182, Cynergy Model 184, the Siemens Model 146‑146A External Pulse G, and the ERM‑101.

All of these devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5

Newest first, rows 1-5 of 5

  • Pacesetter Model 350 Ref K792223

    Class II
    Active 510(k) 510(k) II
  • Cynergy Model 182 Ref K792536

    Class II
    Active 510(k) 510(k) II
  • Cynergy Model 184 Ref K801596

    Class II
    Active 510(k) 510(k) II
  • Siemens Model 146-146A External Pulse G Ref K810566

    Class II
    Active 510(k) 510(k) II
  • Erm-101 Ref K781407

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Cynergy have in the registry?

The registry currently lists 5 devices for Cynergy. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cynergy's devices?

Among its 5 most recently registered devices, Cynergy has devices listed in FDA 510(k) (5 devices).

What risk classes do Cynergy's devices fall under?

Among its 5 most recently registered devices, the classes recorded for Cynergy's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cynergy in the registry?

The most recently registered devices listed for Cynergy include PACESETTER MODEL 350, CYNERGY MODEL 182, CYNERGY MODEL 184 and SIEMENS MODEL 146-146A EXTERNAL PULSE G.

Generated automatically from registry data and not verified by a human reviewer.