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.
Registration Number | 1647149 |
FEI Number | 1000306139 |
Name | STERITEC, INC. |
Owner & Operator | STERITEC, INC. |
Contact Address | 1705 ENTERPRISE ST. -- Athens TX 75751 US |
Official Correspondent |
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Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 1705 ENTERPRISE ST. ATHENS, TX 75751 US |
Establishment Type | Sterilize Medical Device for Another Party (Contract Sterilizer) |
Device Company | Device | Date |
---|---|---|
STERITEC, INC. | RPM Reinforced PTFE Mesh | 2019-05-22 |
STERITEC, INC. | RPM Reinforced PTFE Mesh | 2019-05-22 |
STERITEC, INC. | Teleflex Arrow ON Control single use disposables | 2018-12-05 |
STERITEC, INC. | Teleflex Arrow ON Control single use disposables | 2018-12-05 |
STERITEC, INC. | Endoscopic Injection Needle - CMT | 2017-10-17 |
STERITEC, INC. | Smoke Evacuation | 2013-12-19 |
STERITEC, INC. | Multi-Lead Trial Cable | 2013-12-19 |
STERITEC, INC. | Multi-Lead Trial Cable | 2013-12-19 |
STERITEC, INC. | Laser Waveguide | 2013-12-19 |
STERITEC, INC. | Device, cystometric, Hydraulic | 2013-12-19 |
NCAGE Code | 038T2 | STERITEC INC |
CAGE Code | 038T2 | STERITEC INC |
DUNS | 800118044 | STERITEC INC |