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Forestadent

GermanyFDA 510(k) applicant, unverified

Devices
2

What Forestadent makes

Forestadent manufactures orthodontic bands and expansion screws, which are used in dental applications for aligning teeth and managing jaw growth.

These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Forestadent Orthodontic Bands Ref K925028

    Class I
    Active 510(k) 510(k) I
  • Expansion Screws Ref K925088

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

How many devices does Forestadent have in the registry?

The registry currently lists 2 devices for Forestadent. Devices recorded under merged duplicate company entries are counted once.

Which registries list Forestadent's devices?

Among its 2 most recently registered devices, Forestadent has devices listed in FDA 510(k) (2 devices).

What risk classes do Forestadent's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Forestadent's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Forestadent in the registry?

The most recently registered devices listed for Forestadent include FORESTADENT ORTHODONTIC BANDS and EXPANSION SCREWS.

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