Steri Tek

FDA Filings

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

FDA Registration(s)
Registration Number3012448339
FEI Number3012448339
NameSTERI-TEK
Owner & OperatorSteri-Tek
Contact Address48225 Lakeview Blvd.
Fremont CA 94538 US
Official Correspondent
  • Larry Nichols Nichols
  • x-510-9339700-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address48225 Lakeview Blvd
Fremont, CA 94538 US
Establishment TypeSterilize Medical Device for Another Party (Contract Sterilizer)



FDA Filings

Device
Company
DeviceDate
STERI-TEK
Sentinel CPS2020-04-04
STERI-TEK
NanoFUSE Bioactive Strip2020-01-14
STERI-TEK
NanoFUSE Bioactive Matrix; Bio V BP Bioactive Glass with DBM Putty2020-01-14
STERI-TEK
NanoFUSE Bioactive Matrix; Bio V BP Bioactive Glass with DBM Putty2020-01-14
STERI-TEK
SSPC Delivery Catheter2019-09-25
STERI-TEK
Sentinel CPS2018-12-10
STERI-TEK
Cerafix2018-11-12
STERI-TEK
Restrata2018-11-12
STERI-TEK
IMPEDE Embolization Plug, 7mm2018-07-26
STERI-TEK
IMPEDE Embolization Plug, 5mm2018-07-26
STERI-TEK
IMPEDE Embolization Plug, 10mm2018-07-26
STERI-TEK
Bullfrog? Micro-Infusion Device (Catheter, continuous flush)2018-02-23
STERI-TEK
Blowfish? Transbronchial Micro-Infusion Device (Bronchoscope, flexible or rigid)2018-02-23
STERI-TEK
miLOOP2018-02-23
STERI-TEK
Revolution Suture Passer2017-10-23
STERI-TEK
EntreVu Cannula2016-08-12
STERI-TEK
Latera Absorbable Nasal Implant and Delivery Device2016-08-11
STERI-TEK
AccuLif TL8-12 Implant2016-03-25

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