Reflexonic

FDA Filings

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

FDA Registration(s)

Registration Number	3009129589
FEI Number	3009129589
Name	REFLEXONIC, LLC
Owner & Operator	reflexonic
Contact Address	44055 Riverside Parkway suite 208 Leesburg VA 20176 US
Official Correspondent	kambiz tajkarimi x-202-3218162-202
Registration Status	1
Initial Importer	Y
Registration Expiration	2020-04-25
Registration Address	44055 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	Device	Date
PMN K110566 \| KXQ REFLEXONIC, LLC [reflexonic]	Viberect	2011-07-04