Skip to content

Planmeca USA, Inc.

Country not established

Devices
13

What Planmeca USA, Inc. makes

Planmeca USA, Inc. makes dental devices, including dental units, patient chairs, and radiographic equipment such as panoramic and intraoral devices. Their products include the PM2002 CC, ARISTOCRAT, and DELIGHT, among others.

The company's portfolio is regulated as Class I and Class II devices and is listed in the FDA 510(k) registry. Planmeca USA, Inc. is based in the US.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue13

Newest first, rows 1-13 of 13

Search and filter all 13 devices
Skip device list

  • Admark Ref K923533

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

  • PM2002 Cc, Aristocrat And Aristocrat Deluxe Ref K904947

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

  • Delight Ref K923462

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

  • Pm 2000 Dental Unit Ref K842357

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

  • Planmed Nuance Excel Ref K111361

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

  • PM2002 Proline, PM2002 Proline Ec Ref K923461

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

  • Planmed Sophie Ref K904953

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

  • Automatic Patient Chair PM2000 & A Ref K842359

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

  • Planmeca Sovereign Ref K081699

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

  • Isolight Ref K842358

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

  • Dental Radiographic 90, Model Pm 2002 Cc Panoramic Ref K864474

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

  • PM2002 Cc And PM2002 Ec Ref K904948

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

  • PM2002 Proline Ref K923534

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

Rows 1-13 of 13

Frequently asked questions

How many devices does Planmeca USA, Inc. have in the registry?

The registry currently lists 13 devices for Planmeca USA, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Planmeca USA, Inc.'s devices?

Among its 13 most recently registered devices, Planmeca USA, Inc. has devices listed in FDA 510(k) (13 devices).

What risk classes do Planmeca USA, Inc.'s devices fall under?

Among its 13 most recently registered devices, the classes recorded for Planmeca USA, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Planmeca USA, Inc. in the registry?

The most recently registered devices listed for Planmeca USA, Inc. include ADMARK, PM2002 CC, ARISTOCRAT AND ARISTOCRAT DELUXE, DELIGHT and PM 2000 DENTAL UNIT.

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