Experience Unmatched Precision in Cryoablation
FDA 510(k) cleared cryoablation platform engineered for controlled energy delivery, real-time feedback, and procedure-first workflow design.
Designed for interventional specialists seeking precision and confidence.
Image-Guided Targeting
Target tumors or nerves with precision, minimizing collateral impact
Dual-Mode Freeze Control
User-selectable ablation mode for controlled ice formation
Real-Time Feedback
Live temperature feedback designed to support procedural control
Precision answers for clinical practice
Explore common questions about the Focused Cryotherapy System’s technology, clinical use, and safety.
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The Focused Cryotherapy System is an FDA 510(k)-cleared cryoablation platform consisting of an argon-powered console with image-guidance software and a disposable, dual-mode probe.
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The disposable probe can create either a circumferential or directional ablation zone, selectable in the software.
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Directional cryoablation is a form of cryotherapy that concentrates the ablation zone into a targeted, controllable zone - so clinicians can focus ablation toward the intended anatomy while minimizing impact on surrounding tissue.
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The system continuously monitors temperature at the probe tip and surrounding tissue, enabling clinicians to adjust ablation parameters in real time to optimize safety and outcomes.
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The Focused Cryotherapy System is cleared for use as a cryosurgical tool for cryoablation (cryogenic destruction of tissue) during surgical procedures, within the indications for use specified in the FDA-cleared labeling.
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Intended for use by trained interventional oncologists, radiologists, and surgeons in hospital or outpatient settings; proper training and credentialing are required.
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