This page includes the latest FDA filings for Fabriteq L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3010824458 |
| FEI Number | 3010824458 |
| Name | FABRITEQ LLC |
| Owner & Operator | FabriTEQ |
| Contact Address | 11220 Gilbert Dr Knoxville TN 37932 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 11220 GILBERT DR Knoxville, TN 37932 US |
| Establishment Type | Repack or Relabel Medical Device |
Device Company | Device | Date |
|---|---|---|
FABRITEQ LLC [FabriTEQ] | SpO2 Sensor Wrap | 2019-12-19 |
| NCAGE Code | 7QBQ7 | FABRITEQ LLC!DBA FABRITEQ |
| CAGE Code | 7QBQ7 | FABRITEQ LLC FABRITEQ |
| S.A.M. Registration | 7QBQ7 [79307777] | FABRITEQ LLC FABRITEQ |