Steritec Inc

FDA Filings

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

FDA Registration(s)
Registration Number1647149
FEI Number1000306139
NameSTERITEC, INC.
Owner & OperatorSTERITEC, INC.
Contact Address1705 ENTERPRISE ST. --
Athens TX 75751 US
Official Correspondent
  • CHARLES G JENKINS
  • x-903-6773950-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1705 ENTERPRISE ST.
ATHENS, TX 75751 US
Establishment TypeSterilize Medical Device for Another Party (Contract Sterilizer)



FDA Owner/Operator Registration

FDA Filings

Device
Company
DeviceDate
STERITEC, INC.
RPM Reinforced PTFE Mesh2019-05-22
STERITEC, INC.
RPM Reinforced PTFE Mesh2019-05-22
STERITEC, INC.
Teleflex Arrow ON Control single use disposables2018-12-05
STERITEC, INC.
Teleflex Arrow ON Control single use disposables2018-12-05
STERITEC, INC.
Endoscopic Injection Needle - CMT2017-10-17
STERITEC, INC.
Smoke Evacuation2013-12-19
STERITEC, INC.
Multi-Lead Trial Cable2013-12-19
STERITEC, INC.
Multi-Lead Trial Cable2013-12-19
STERITEC, INC.
Laser Waveguide2013-12-19
STERITEC, INC.
Device, cystometric, Hydraulic2013-12-19

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