Biowave Corp

FDA Filings

This page includes the latest FDA filings for Biowave Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3004558433
FEI Number3004558433
NameBIOWAVE CORPORATION
Owner & OperatorBIOWAVE CORPORATION
Contact Address8 KNIGHT STREET, Suite 201 --
Norwalk CT 06851 US
Official Correspondent
  • Bradford - Siff
  • x-203-6357175-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address8 KNIGHT STREET Suite 201
NORWALK, CT 06851 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
BioWave Corporation
BioWave BioWraps2021-07-08
BioWave Corporation
BioWaveGO RX2021-02-24
BIOWAVE CORPORATION
Biowave Percutaneous Electrodes 2019-12-23
BIOWAVE CORPORATION
Biowave Percutaneous Electrodes 2019-12-23
BIOWAVE CORPORATION
BiowavePRO 2019-12-23
BIOWAVE CORPORATION
BioWaveGO2019-12-18
BIOWAVE CORPORATION
BiowaveHOME 2019-10-23
Biowave Corporation
BioWaveGO2018-08-17
BIOWAVE CORPORATION
Biowave Noninvasive Electrodes 2018-03-29
BIOWAVE CORPORATION
Biowave Noninvasive Electrodes 2018-03-29
BIOWAVE CORPORATION
Biowave Noninvasive Electrodes 2018-03-29
BIOWAVE CORPORATION
BioWaveHOME2015-11-19
BIOWAVE CORPORATION
BiowaveHOME Neuromodulation Pain Therapy Device2015-09-25
BIOWAVE CORPORATION
HOMEWAVE NEUROMODULATIONS PAIN THERAPY DEVICE2008-02-01
BIOWAVE CORPORATION
BioWavePENS2007-04-10
BIOWAVE CORPORATION
BioWavePENS2007-04-10
BIOWAVE CORPORATION
DEEPWAVE PERCUTANEOUS NEUROMODULATION PAIN THERAPY SYSTEM2006-08-15
BIOWAVE CORPORATION
DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE2005-12-13

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