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Octicon Corp.

United StatesFDA applicant, unverified

Devices
2

What Octicon Corp. makes

Octicon Corp. manufactures hearing aids, including the OTICON E25P and E-27P models, designed for auditory assistance in adults.

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

  • Oticon, E25P Ref K830435

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Oticon, E-27P Ref K830436

    Active Regimes: 510(k) Registry: 510(k) Class:I

Frequently asked questions

How many devices does Octicon Corp. have in the registry?

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

Which registries list Octicon Corp.'s devices?

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

What risk classes do Octicon Corp.'s devices fall under?

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

What are the newest devices from Octicon Corp. in the registry?

The most recently registered devices listed for Octicon Corp. include OTICON, E25P and OTICON, E-27P.

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