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Pacific Rim Dental, Inc.

United StatesFDA applicant, unverified

Devices
2

What Pacific Rim Dental, Inc. makes

Pacific Rim Dental, Inc. makes dental devices including the RE NU and GENESIS products.

These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Re Nu Ref K973289

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Genesis Ref K972871

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

Frequently asked questions

How many devices does Pacific Rim Dental, Inc. have in the registry?

The registry currently lists 2 devices for Pacific Rim Dental, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Pacific Rim Dental, Inc.'s devices?

Among its 2 most recently registered devices, Pacific Rim Dental, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Pacific Rim Dental, Inc.'s devices fall under?

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

What are the newest devices from Pacific Rim Dental, Inc. in the registry?

The most recently registered devices listed for Pacific Rim Dental, Inc. include RE NU and GENESIS.

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