Is this your brand? Sign in to claim ownership.
Sign in to claim this brandAktina 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
- linkedin.com/company/aktina-medical
- facebook.com/AktinaMedical
- [email protected]
- Phone
- +1 845 268 0101
- PRRC Contact
- Tony Spaccarotella
- EUDAMED SRN
- US-MF-000005935
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (125)
Page 1 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| PinPoint Accessory | 50-120 | EUDAMED | Class I | Active |
| Reticle Siemens | 54-224 | EUDAMED | Class I | Active |
| Port Film Graticule Siemens | 54-045 | EUDAMED | Class I | Active |
| PinPoint Accessory | 50-255 | EUDAMED | Class I | Active |
| Beam Block Siemens | 56-000-HA | EUDAMED | Class I | Active |
| PositionPro Component | 50-855 | EUDAMED | Class I | Active |
| CT Overlay | 11-465BR | EUDAMED | Class I | Active |
| PinPoint Accessory | 50-126 | EUDAMED | Class I | Active |
| PInPoint System | 50-520 | EUDAMED | Class IIa | Active |
| Port Film Graticule Elekta | 11-344 | EUDAMED | Class I | Active |
| PinPoint System | 50-807 | EUDAMED | Class IIa | Active |
| PInPoint System | 50-470 | EUDAMED | Class IIa | Active |
| PinPoint Accessory | 50-107 | EUDAMED | Class I | Active |
| Table Top Accessory Elekta | 11-213 | EUDAMED | Class I | Active |
| Table Top Accessory Elekta | 11-215 | EUDAMED | Class I | Active |
| Active Breathing Coordinator | K131313 | FDA 510(k) | Class II | Active |
| Interlocked Circular Small Field Collimators, Elekta Integrated | K161984 | FDA 510(k) | Class II | Active |
| Active Breathing Coordinator | K151097 | FDA 510(k) | Class II | Active |
| Port Film Graticule Siemens | 54-044 | EUDAMED | Class I | Active |
| Beam Block Siemens | 54-000-SL | EUDAMED | Class I | Active |
| AK550 Table Top | 51-200 | EUDAMED | Class I | Active |
| Thermoplastic Mask | 40-721 | EUDAMED | Class I | Active |
| Siemens Wedge | 56-300-MX15 | EUDAMED | Class I | Active |
| Thermoplastic Mask | 40-731 | EUDAMED | Class I | Active |
| Beam Block Siemens | 52-485 | EUDAMED | Class I | Active |
| Arm Cradle | 60-812 | EUDAMED | Class I | Active |
| CT Overlay | 11-469 | EUDAMED | Class I | Active |
| Beam Block Siemens | 54-000-HL | EUDAMED | Class I | Active |
| Beam Block Siemens | 57-901 | EUDAMED | Class I | Active |
| Reticle Siemens | 54-227 | EUDAMED | Class I | Active |
| Beam Block Siemens | 56-000-HL | EUDAMED | Class I | Active |
| Table Top Accessory Elekta | 11-330 | EUDAMED | Class I | Active |
| Wedge Filter Elekta | 11-495-45 | EUDAMED | Class I | Active |
| Aktina Breathing Coordinator Control Module | 12-200-01 | EUDAMEDFDA UDI | Class IIb | Active |
| Small Field Collimator, Elekta | 50-302-390 | EUDAMED | Class I | Active |
| Beam Block Elekta | 11-563 | EUDAMED | Class I | Active |
| Beam Block Elekta | 11-290 | EUDAMED | Class I | Active |
| Small Field Collimator, Elekta | 50-302-340 | EUDAMED | Class I | Active |
| Table Top Accessory Siemens | 52-212 | EUDAMED | Class I | Active |
| Thermoplastic Mask | 40-741 | EUDAMED | Class I | Active |
| Cassette Holder | 11-235 | EUDAMED | Class I | Active |
| PinPoint Accessory | 50-130 | EUDAMED | Class I | Active |
| Winston-Lutz Marker | 50-335 | EUDAMED | Class I | Active |
| PInPoint System | 50-460 | EUDAMED | Class IIa | Active |
| Beam Block Elekta | 11-560 | EUDAMED | Class I | Active |
| Thermoplastic Mask | 40-723 | EUDAMED | Class I | Active |
| Front Pointer Elekta | 11-360 | EUDAMEDFDA UDI | Class I | Active |
| Thermoplastic Mask | 40-722 | EUDAMED | Class I | Active |
| Siemens Wedge | 56-300-MI45 | EUDAMED | Class I | Active |
| Thermoplastic Mask | 40-732 | EUDAMED | Class I | Active |
Related Companies
Authorised Representatives
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.