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L A P GMBH LASER APPLIKATIONEN

US

Last updated May 23, 2026

What L A P GMBH LASER APPLIKATIONEN makes

The company manufactures anthropomorphic phantoms and positioning systems for therapeutic radiation and radiological imaging. These include multi-modality phantoms like the EASY CUBE and EASY SLAB, designed for testing and calibration, as well as patient positioning systems such as the DORADO and CARINA for laser alignment and video camera tracking.

The portfolio includes devices classified as Class I and Class II under regulatory frameworks, with listings in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does L A P GmbH Laser Applikationen manufacture?

L A P GmbH Laser Applikationen specializes in devices used for therapeutic radiation and radiological imaging. Their portfolio includes anthropomorphic phantoms—such as the EASY CUBE and EASY SLAB—which simulate human anatomy for testing and calibration across multiple modalities. They also produce patient positioning systems like the DORADO (laser alignment) and CARINA (radiological video camera tracking), designed to improve precision in treatment and imaging procedures.

Where is L A P GmbH Laser Applikationen based?

The company is based in the United States. While their headquarters location isn’t specified, their regulatory listings (e.g., FDA UDI) confirm their operational presence in the country.

Which regulatory registries list L A P GmbH Laser Applikationen’s devices?

L A P GmbH Laser Applikationen’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry tracks authorized medical devices in the U.S., ensuring traceability and compliance for products like phantoms and positioning systems.

How are L A P GmbH Laser Applikationen’s devices classified under regulatory frameworks?

The company’s devices fall into Class I and Class II classifications. Class I typically includes low-risk devices like some phantoms or positioning aids, while Class II covers those with moderate risk (e.g., devices requiring performance standards or special controls). Classification depends on factors like intended use and potential patient risk.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
313586582

Catalogue (201)

Page 5 of 5
DeviceModel / ReferenceRegistriesClassStatus
Easy Slab Adapter Plate IBA NACP type
FDA UDI
Class IActive

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