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The Axxent eBx system is FDA-cleared and CE marked, in use at over 120 sites in 16 countries for early-stage breast, skin, gynecological, and brain cancers, with emerging data for other indications. Published clinical results support safety, convenience (single-session IORT), and efficacy comparable to traditional approaches, especially for early-stage breast cancer and nonmelanomatous cutaneous malignancies.
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