Public source

Reviewed 10 Nov 2026

Completeness Fair (31%)

Synchrony

Accuray

No papers to support — we monitor for new evidence.

Key features

Motion tracking

General Information

Product name

Synchrony

Company

Workflow phase

Treatment

Modality

x-ray

Treatment site

Not specified

Exact structures

Not specified

Regulatory Information

CE Certification

Pathway:

MDR

Class:

Class IIb

Verified by Health AI Register

FDA Certification

Pathway:

510(k) cleared

Class:

Class II

FDA Number:

K120233 and K182687

View FDA record

Verified by Health AI Register

Other certifications

Not specified

Evidence & Research

No research papers or evidence on file yet.

The registry monitors publications for new evidence.

Technical Specifications

Prerequisites

Specific hardware required

Defined prerequisite(s)

CyberKnife® or Radixact® System

Treatment technique

Not specified

Delivery system

Cyberknife, Radixact

Workflow features

Motion management

Patient population age

Not specified

Input

Not specified

Input format

Not specified

Output

Not specified

Output format

Not specified

Integration

Embedded in hardware

Integration method

Not specified

API documentation availability

Not specified

API documentation, if publicly available

Not specified

TPS compatibility

Not specified

Deployment

Not specified

Trigger for AI functionality

Not specified

Processing time

Not specified

Retraining locally

Not applicable

Claims

Not specified

Known limitations

Not specified

Market Presence

On market since

Not specified

AI Platforms

Resellers

Not specified

Countries present

Not specified

Paying clinical customers

Not specified

Research/test users

Not specified

Pricing Information

Pricing model

Not specified

Based on

Not specified

Source: Public | First published: Nov 10, 2026 | Last updated: Nov 10, 2026