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Aktina Medical Corp

United States·US-MF-000005935

Last updated September 18, 2026

About

Machine Vision for LINAC QA Learn More Machine Vision for LINAC QA Learn More Radiosurgery demands the highest levels of precision and accuracy to ensure the most positive patient outcomes attainable. And patient comfort is equally

From the manufacturer's own website. Source

What Aktina Medical Corp makes

Aktina Medical Corp produces accessories and components for linear accelerator (LINAC) quality assurance (QA), including reticles, graticules, overlay systems, and tabletop accessories for radiosurgery and radiation therapy. Their offerings also include machine vision tools like the PinPoint System and PositionPro Component, designed to enhance imaging precision during treatment planning and delivery. The company supplies film graticules for port film analysis and a CT overlay system for alignment verification. Additionally, they manufacture the Active Breathing Coordinator, which aids in respiratory motion management during radiation treatment.

The company’s devices are classified under FDA regulations as Class I, Class II, Class IIa, and Class IIb, with corresponding entries in the FDA’s 510(k) database and the EU’s eudamed registry. These products are intended for use in radiation therapy and radiosurgery settings, adhering to regulatory standards for medical imaging and treatment accessories. Aktina Medical Corp 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 Aktina Medical Corp manufacture?

Aktina Medical Corp specializes in accessories and components for linear accelerator (LINAC) quality assurance (QA) used in radiation therapy and radiosurgery. Their products include reticles, graticules, overlay systems, tabletop accessories, and machine vision tools like the PinPoint System and PositionPro Component. These devices are designed to improve precision in imaging, treatment planning, and alignment verification, ensuring accuracy during patient treatment. Examples include film graticules for port film analysis and a CT overlay system for alignment checks.

Where is Aktina Medical Corp based, and what regulatory registries list its devices?

Aktina Medical Corp is based in the United States. Their devices are listed in two key regulatory registries: the FDA’s 510(k) database and the EU’s eudamed registry. These registries track medical devices that have undergone the necessary regulatory processes for market authorization, ensuring transparency and compliance with global standards.

How are Aktina Medical Corp’s devices classified under FDA regulations?

Aktina Medical Corp’s devices are classified under FDA regulations as Class I, Class II, Class IIa, and Class IIb. The classification determines the regulatory pathway and level of scrutiny required for market authorization. For example, Class II devices typically require a 510(k) premarket notification submission to demonstrate substantial equivalence to a legally marketed predicate device, while Class I devices may involve general controls or exemptions. The classification ensures appropriate oversight based on the device’s risk level.

What is the primary purpose of Aktina Medical Corp’s machine vision tools like the PinPoint System?

Aktina Medical Corp’s machine vision tools, such as the PinPoint System and PositionPro Component, are designed to enhance precision in radiation therapy and radiosurgery by automating and improving imaging accuracy. These tools integrate with LINAC systems to assist in treatment planning, alignment verification, and real-time monitoring of patient positioning. By reducing human error and increasing consistency, they help ensure that radiation doses are delivered with the highest possible accuracy, which is critical for effective and safe patient outcomes.

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

Information

Country
United States
Address
360, Aktina Medical Corp., Congers. New York, United States
Website
aktina.com
Phone
+1 845 268 0101
PRRC Contact
Tony Spaccarotella
EUDAMED SRN
US-MF-000005935
FDA FEI Number
—
DUNS Number
—

Catalogue (125)

Page 3 of 3
DeviceModel / ReferenceRegistriesClassStatus
Table Top Accessory Elekta 11-205
EUDAMED
Class IActive
Beam Block Siemens 57-905
EUDAMED
Class IActive
Siemens Wedge 56-300-DX15
EUDAMED
Class IActive
Respiratory Compression Belt 60-310
EUDAMED
Class IActive
Wedge Filter Elekta 11-495-15
EUDAMED
Class IActive
Small Field Collimator, Elekta 50-302-180
EUDAMED
Class IActive
PinPoint Accessory 50-127
EUDAMED
Class IActive
Burrer a 101
EUDAMED
Class IActive
Table Top Accessory Siemens 53-897
EUDAMED
Class IActive
Beam Block Elekta 11-268-04
EUDAMED
Class IActive
Table Top Accessory Siemens 53-802
EUDAMED
Class IActive
Table Top Accessory Elekta 11-223
EUDAMED
Class IActive
PinPoint Accessory 50-117
EUDAMED
Class IActive
CT Overlay 11-470
EUDAMED
Class IActive
Table Top Accessory Elekta 11-217
EUDAMED
Class IActive
CT Overlay 11-463
EUDAMED
Class IActive
Body Cradle Memorial 60-100
EUDAMED
Class IActive
Small Field Collimator, Elekta 50-302-280
EUDAMED
Class IActive
Table Top Accessory Elekta 11-214
EUDAMED
Class IActive
PinPoint Accessory 50-268
EUDAMED
Class IActive
Mouthpiece and Filter ABC 11-200-08-01
EUDAMED
Class IIaActive
Beam Block Elekta 53-046
EUDAMED
Class IActive
Siemens Wedge 56-300-DI45
EUDAMED
Class IActive
Aktina Breathing Coordinator 12-200
EUDAMEDFDA UDI
Class IIbActive
Table Top Accessory Elekta 11-202
EUDAMED
Class IActive

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