Biowave Corporation
Biowave Corporation holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2026.
Top product codes for Biowave Corporation
Recent clearances by Biowave Corporation
- K261522 — BioWave BioWraps
- K203158 — BioWave BioWraps
- K210202 — BioWaveGO RX
- K180943 — BioWaveGO
- K152437 — BiowaveHOME Neuromodulation Pain Therapy Device
- K072123 — HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE
- K061166 — DEEPWAVE PERCUTANEOUS NEUROMODULATION PAIN THERAPY SYSTEM
- K052289 — DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.