FDA Device Intelligence
HomeDevice types › GZJ

Stimulator, Nerve, Transcutaneous, For Pain Relief

FDA product code GZJ · Class 2 · Neurology

1,296
Registered devices
500
Adverse events
7
Recalls
606
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2011-02-07Neuro Resource Group IncProduct package contains alcohol prep pads recalled by Triad Group because the prep pads have the potential to be contaminated with an objectionable organism.
2008-07-18Synaptic CorpDevice was distributed without marketing approval.
2007-06-29Avazzia, IncPlastic Cases may crack due to manufacturing by the supplier not meeting specifications
2007-06-29Avazzia, IncPlastic Cases may crack due to manufacturing by the supplier not meeting specifications
2007-06-29Avazzia, IncPlastic Cases may crack due to manufacturing by the supplier not meeting specifications
2007-06-29Avazzia, IncPlastic Cases may crack due to manufacturing by the supplier not meeting specifications
2003-05-23RehabilicareIf there was a short, excessive heat could have been generated in the transformer due to the use of the wrong fuse.

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