This page includes the latest FDA filings for Interx Technologies. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3004786509 |
| FEI Number | 3004786509 |
| Name | InterX Technologies |
| Owner & Operator | InterX Technologies |
| Contact Address | 870 N Dorothy Dr. Suite 708 Richardson TX 75081 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 870 N Dorothy Dr Ste 708 Richardson, TX 75081 US |
| Establishment Type | Repack or Relabel Medical Device |
Device Company | Device | Date |
|---|---|---|
| Interx Technologies | InterX 1589-001 | 2021-02-19 |
| Interx Technologies | InterX 1075-001 | 2021-02-19 |
| Interx Technologies | InterX 1475-001 | 2021-02-19 |
| Interx Technologies | InterX 1507-001 | 2021-02-19 |
| Interx Technologies | InterX 1538-001 | 2021-02-19 |
| Interx Technologies | InterX 1072-001 | 2021-02-19 |
| Interx Technologies | InterX 1674-001 | 2021-02-19 |
| Interx Technologies | InterX 1569-001 | 2021-02-19 |
| Interx Technologies | InterX 1220-001 | 2021-02-19 |
| Interx Technologies | InterX 1155-001 | 2021-02-19 |
| Interx Technologies | InterX 1070-001 | 2021-02-19 |
InterX Technologies | InterX 1000/Derma 200 Stimulator For Cosmetic Use | 2020-02-26 |
InterX Technologies | InterX 1000/Derma 200 Stimulator For Cosmetic Use | 2020-02-26 |
| Interx Technologies | InterX 1478-001 | 2019-10-23 |
| Interx Technologies | InterX 1150-001 | 2019-10-23 |
| Interx Technologies | InterX 1149-001 | 2019-10-23 |
| Interx Technologies | InterX 1141-001 | 2019-10-23 |
| Interx Technologies | InterX 1140-001 | 2019-10-23 |
InterX Technologies | InterX Self-Adhesive Dual Electrode - Non-Sterile | 2016-03-01 |
InterX Technologies | InterX500 Flexible Array Electrode | 2016-03-01 |
InterX Technologies | InterX5000 | 2016-03-01 |