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. |