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3 Lesion NT1100 Pain Management RF Generator
No active recall
FDA product code: GXD · Category: Generator, Lesion, Radiofrequency
Severity Snapshot
135 total reports2016-02 – 2024-11 date range12.6% physician / facility reported87.4% manufacturer reported1 SKU variants
Reporting Trend
Annual Reporting Volume
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Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.
Reported Events
Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.
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