This page includes the latest FDA filings for Promedtek Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3007134923 |
| FEI Number | 3007134923 |
| Name | PROMEDTEK, INC. |
| Owner & Operator | ProMedTek, Inc. |
| Contact Address | 4110 N Scottsdale Road Suite 270 Scottsdale AZ 85251 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 4110 N Scottsdale Rd Ste 270 Scottsdale, AZ 85251 US |
| Establishment Type | Develop Specifications But Do Not Manufacture At This Facility |
Device Company | Device | Date |
|---|---|---|
| PROMEDTEK, INC. | Replexa+ Treatment Applicator | 2019-07-16 |
| PROMEDTEK, INC. | Replexa+ Device | 2019-07-16 |
PROMEDTEK, INC. | Replexa+ | 2016-12-26 |
PROMEDTEK INC. | ProMedTek Model C1400 Shortwave Diathermy Device | 2016-11-17 |
PROMEDTEK, INC. | MODEL PMT850 | 2007-05-24 |
| NCAGE Code | 4V5F1 | PROMEDTEK, INC. |
| NCAGE Code | 06BG7 | PROMEDTEK INC!DBA REIDEL IMAGING |
| CAGE Code | 06BG7 | PROMEDTEK INC REIDEL IMAGING |
| CAGE Code | 4V5F1 | PROMEDTEK, INC. |
| S.A.M. Registration | 4V5F1 [604679527] | PROMEDTEK, INC. |
| DUNS | 187851506 | Promedtek Inc |
| SEC | 0001334026 | PROMEDTEK INC |