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Diversified Products, Inc.

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Diversified Products, Inc. is a medical device manufacturer, with 1,171 devices listed in FDA GUDID (FDA Class I) as of 12 Nov 2026.

Devices
1,171

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 1,171
Device classes
  • FDA Class I 1,171
Identifiers
  • DUNS 604170506

What Diversified Products, Inc. makes

Diversified Products, Inc. manufactures magnifying spectacles designed for reading and visual clarity, including models like Clear Readers, VK Couture, Optitek, SAV, and Flex. These devices are intended for individuals requiring enhanced magnification for near-vision tasks, such as reading or detailed work.

The company’s products are classified as Class I medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to applicable U.S. regulatory standards for these devices.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1,171

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Company details

DUNS number
604170506

Frequently asked questions

How many devices does Diversified Products, Inc. have in the registry?

The registry currently lists 1171 devices for Diversified Products, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Diversified Products, Inc.'s devices?

Among its 50 most recently registered devices, Diversified Products, Inc. has devices listed in FDA GUDID (50 devices).

What risk classes do Diversified Products, Inc.'s devices fall under?

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

What are the newest devices from Diversified Products, Inc. in the registry?

The most recently registered devices listed for Diversified Products, Inc. include Clear Readers 1111-200-ME, VK Couture 1303V-250, Optitek AR7264-175-ME and SAV 2101-250-CA.

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