This page includes the latest FDA filings for Ascentron Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3013069546 |
| FEI Number | 3013069546 |
| Name | ASCENTRON, INC. |
| Owner & Operator | Ascentron, Inc. |
| Contact Address | 994 Antelope Rd. White City OR 97503 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 994 Antelope Rd. White City, OR 97503 US |
| Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
|---|---|---|
ASCENTRON, INC. | Thermostim accessories | 2019-11-20 |
ASCENTRON, INC. | Thermostim accessories | 2019-11-20 |
ASCENTRON, INC. | Light pad and Light probe | 2019-11-20 |
ASCENTRON, INC. | Dynatron Solaris Series (model numbers 709, 708, 706, and 705) | 2019-04-01 |
ASCENTRON, INC. | Dynatron Solaris Series (model numbers 709, 708, 706, and 705) | 2019-04-01 |
ASCENTRON, INC. | Dynatron Solaris Series (model numbers 709, 708, 706, and 705) | 2019-04-01 |
ASCENTRON, INC. | Dynatron Solaris Series (model numbers 709, 708, 706, and 705) | 2019-04-01 |
ASCENTRON, INC. | Dynatron Solaris Series (model numbers 709, 708, 706, and 705) | 2019-04-01 |
| NCAGE Code | 5UKU2 | ASCENTRON INC. |
| CAGE Code | 5UKU2 | ASCENTRON INC. |
| S.A.M. Registration | 5UKU2 [109140249] | ASCENTRON INC. |
| DUNS | 109140249 | ASCENTRON INC. |