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.
Registration Number | 3012448339 |
FEI Number | 3012448339 |
Name | STERI-TEK |
Owner & Operator | Steri-Tek |
Contact Address | 48225 Lakeview Blvd. Fremont CA 94538 US |
Official Correspondent |
|
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 48225 Lakeview Blvd Fremont, CA 94538 US |
Establishment Type | Sterilize Medical Device for Another Party (Contract Sterilizer) |
Device Company | Device | Date |
---|---|---|
STERI-TEK | Sentinel CPS | 2020-04-04 |
STERI-TEK | NanoFUSE Bioactive Strip | 2020-01-14 |
STERI-TEK | NanoFUSE Bioactive Matrix; Bio V BP Bioactive Glass with DBM Putty | 2020-01-14 |
STERI-TEK | NanoFUSE Bioactive Matrix; Bio V BP Bioactive Glass with DBM Putty | 2020-01-14 |
STERI-TEK | SSPC Delivery Catheter | 2019-09-25 |
STERI-TEK | Sentinel CPS | 2018-12-10 |
STERI-TEK | Cerafix | 2018-11-12 |
STERI-TEK | Restrata | 2018-11-12 |
STERI-TEK | IMPEDE Embolization Plug, 7mm | 2018-07-26 |
STERI-TEK | IMPEDE Embolization Plug, 5mm | 2018-07-26 |
STERI-TEK | IMPEDE Embolization Plug, 10mm | 2018-07-26 |
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 | miLOOP | 2018-02-23 |
STERI-TEK | Revolution Suture Passer | 2017-10-23 |
STERI-TEK | EntreVu Cannula | 2016-08-12 |
STERI-TEK | Latera Absorbable Nasal Implant and Delivery Device | 2016-08-11 |
STERI-TEK | AccuLif TL8-12 Implant | 2016-03-25 |