Mainstream Medical Devices

FDA Filings

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

FDA Registration(s)
Registration Number3016112537
FEI Number3016112537
NameMAINSTREAM MEDICAL DEVICES
Owner & OperatorMainstream Medical Devices
Contact Address3913 Todd Lane Suite 304
Austin TX 78744 US
Official Correspondent
  • Dana Wilcox
  • 01-512-2893437-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3913 Todd Lane Suite 304
Austin, TX 78744 US
Establishment Type
  • Complaint File Establishment per 21 CFR 820.198
  • Repack or Relabel Medical Device



FDA Filings

Device
Company
DeviceDate
MAINSTREAM MEDICAL DEVICES
Gastro-Test2019-11-20
MAINSTREAM MEDICAL DEVICES
Mainstream Medical Surgical Knife2019-11-20

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