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Micropos Medical AB

US

Last updated May 23, 2026

What Micropos Medical AB makes

Micropos Medical AB manufactures the RayPilot System, a medical device designed for precise radiation therapy guidance and real-time imaging during procedures.

The RayPilot System is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in 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 Micropos Medical AB manufacture?

Micropos Medical AB specializes in the RayPilot System, a medical device used for guiding radiation therapy with real-time imaging. This system is intended to enhance precision during procedures by providing accurate visual feedback.

Where is Micropos Medical AB based?

Micropos Medical AB is headquartered in the United States. The company’s location is relevant for regulatory compliance and device distribution within the region.

How are the devices manufactured by Micropos Medical AB classified under FDA regulations?

The RayPilot System is classified as a Class II medical device by the FDA. This classification typically indicates moderate risk, requiring specific controls to ensure safety and effectiveness. The company submits its devices through the 510(k) pathway, which demonstrates substantial equivalence to a legally marketed predicate device.

Which regulatory registries or databases list Micropos Medical AB’s devices?

Micropos Medical AB’s RayPilot System is listed in the FDA’s 510(k) registry, which tracks devices cleared through the 510(k) pathway. This registry helps healthcare providers, regulators, and researchers verify the device’s regulatory status and compliance.

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

Information

Country
US
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Catalogue (13)

DeviceModel / ReferenceRegistriesClassStatus
Raypilot Quality Control Kit 1
FDA UDI
Class IIActive
Raypilot Receiver 1
FDA UDI
Class IIActive
Raypilot System Cable 1
FDA UDI
Class IIActive
Raypilot Hypocath 1
FDA UDI
Class IIActive
Raypilot Extension Plate 1
FDA UDI
Class IIActive
Raypilot Transmitter Cable 1
FDA UDI
Class IIActive
Raypilot Matching Network 1
FDA UDI
Class IIActive
Raypilot Transmitter Tester 1
FDA UDI
Class IIActive
Raypilot Power Box 1
FDA UDI
Class IIActive
Raypilot Table Displacement Meter 1
FDA UDI
Class IIActive
Raypilot Software 1
FDA UDI
Class IIActive
Raypilot Viewcath 1
FDA UDI
Class IIActive
RayPilot System K203722
FDA 510(k)
Class IIActive

Related Companies

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Micropos Medical Ab Goteborg Vastra Gotaland · SE FEI 3026961165