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Dyna Flex

Country not established

Devices
4

What Dyna Flex makes

Dyna Flex manufactures orthodontic appliances, including fixed bracket systems and associated components like brackets and buttons designed for dental alignment.

The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) pathway. Dyna Flex operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

  • DynaFlex Ref K190583

    Class II
    Active 510(k) 510(k) II
  • Dynaflex Ref K121396

    Class II
    Active 510(k) 510(k) II
  • DynaFlex Clear Brackets & Buttons Ref K230225

    Class II
    Active 510(k) 510(k) II
  • Dynaflex Ref K103076

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

Frequently asked questions

How many devices does Dyna Flex have in the registry?

The registry currently lists 4 devices for Dyna Flex. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dyna Flex's devices?

Among its 4 most recently registered devices, Dyna Flex has devices listed in FDA 510(k) (4 devices).

What risk classes do Dyna Flex's devices fall under?

Among its 4 most recently registered devices, the classes recorded for Dyna Flex's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Dyna Flex in the registry?

The most recently registered devices listed for Dyna Flex include DynaFlex and DynaFlex Clear Brackets & Buttons.

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