This page includes the latest FDA filings for Vitaldyne Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3003697998 |
| FEI Number | 3003697998 |
| Name | VITALDYNE, INC. |
| Owner & Operator | VITALDYNE, INC. |
| Contact Address | 400 Cokato Street E Cokato MN 55321 US |
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 400 COKATO ST E Cokato, MN 55321 US |
| Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
|---|---|---|
VITALDYNE, INC. | Microtaper Safety Introducer Set | 2019-04-17 |
| NCAGE Code | 1TC23 | VITALDYNE, INC.!DBA TWIN RIVER TECHNOLOGY |
| NCAGE Code | 6XRU6 | VITALDYNE, INC.!DBA TWIN RIVER TECHNOLOGY USE CAGE!CODE 1TC23 FOR CATALOGING |
| CAGE Code | 1TC23 | VITALDYNE, INC. TWIN RIVER TECHNOLOGY |
| CAGE Code | 6XRU6 | VITALDYNE, INC. TWIN RIVER TECHNOLOGY USE CAGE CODE 1TC23 FOR CATALOGING |
| DUNS | 005865147 | Vitaldyne, Inc. |