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Stimulator, Peripheral Nerve, Implanted (Pain Relief)

FDA product code GZF · Class 2 · Neurology

423
Registered devices
4,474
Adverse events
7
Recalls
24
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-06-03Nalu Medical, Inc.Neurostimulation Systems have a manufacturing non-conformance that may reduce the efficiency of the radiofrequency signals between the Implantable Pulse Generat
2020-07-15Stimwave Technologies IncThe product contains a non-functional component not referenced in product labeling.
2020-07-15Stimwave Technologies IncThe product contains a non-functional component not referenced in product labeling.
2020-07-15Stimwave Technologies IncThe product contains a non-functional component not referenced in product labeling.
2020-07-15Stimwave Technologies IncThe product contains a non-functional component not referenced in product labeling.
2020-07-15Stimwave Technologies IncThe product contains a non-functional component not referenced in product labeling.
2020-07-15Stimwave Technologies IncThe product contains a non-functional component not referenced in product labeling.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.