ClearanceBrief
Company ยท US

Biowave Corporation

FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2026. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GZJStimulator, Nerve, Transcutaneous, For Pain Relief4
GXYElectrode, Cutaneous2
LIHInterferential Current Therapy1
NHIStimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 3, 2026K261522BioWave BioWraps
Biowave Corporation
GXY
Jul 8, 2021K203158BioWave BioWraps
Biowave Corporation
GXY
Feb 24, 2021K210202BioWaveGO RX
Biowave Corporation
GZJ
Aug 17, 2018K180943BioWaveGO
Biowave Corporation
GZJ
Sep 25, 2015K152437BiowaveHOME Neuromodulation Pain Therapy Device
Biowave Corporation
GZJ
Feb 1, 2008K072123HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE
Biowave Corporation
GZJ
Aug 15, 2006K061166DEEPWAVE PERCUTANEOUS NEUROMODULATION PAIN THERAPY SYSTEM
Biowave Corporation
NHI
Dec 13, 2005K052289DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE
Biowave Corporation
LIH

Latest recalls

DateFirm and productCodeLinked 510(k)
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