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Oticon Corp.

Also registered as Oticon, Inc.

United StatesFDA applicant, unverified FDA FEI 2240713

Devices
66
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue66

Newest first, rows 1-50 of 66

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Rows 1-50 of 66

Showing 1-50 of 66

Company details

FDA FEI number
2240713
Address
580 Howard Avenue, SOMERSET, NJ, 08873

Frequently asked questions

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

The registry currently lists 66 devices for Oticon Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Oticon Corp.'s devices?

Among its 50 most recently registered devices, Oticon Corp. has devices listed in FDA 510(k) (50 devices).

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

Among its 50 most recently registered devices, the classes recorded for Oticon Corp.'s devices are Class I. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Oticon Corp. include OTICON, E26P, CUSTOM IN-THE-CANAL (ITC) HEARING AID MODEL I54, BTE HEARING AID OTICON MODEL E39PL and OTICON EARETTE HEARING AID #E17CF.

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