Reflexonic L L C

FDA Filings

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

FDA Registration(s)
Registration Number3009129589
FEI Number3009129589
NameREFLEXONIC, LLC
Owner & Operatorreflexonic
Contact Address44055 Riverside Parkway suite 208
Leesburg VA 20176 US
Official Correspondent
  • kambiz tajkarimi
  • x-202-3218162-202
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address44055 Riverside Parkway suite 208
Lansdowne, VA 20176 US
Establishment Type
  • Develop Specifications But Do Not Manufacture At This Facility
  • Repack or Relabel Medical Device

FDA Filings

Device
Company
DeviceDate
REFLEXONIC, LLC
Viberect Penile Vibratory Stimulation Device2014-10-03
REFLEXONIC, LLC [reflexonic]
Viberect2011-07-04
REFLEXONIC, LLC
VIBERECT PENILE VIBRATORY STIMULATION DEVICE2011-06-24

Related Finance Registrations
NCAGE Code6RY70REFLEXONIC, LLC
CAGE Code6RY70REFLEXONIC, LLC
DUNS035047956REFLEXONIC, LLC
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.