This page includes the latest FDA filings for Resoundant Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3013695852 |
FEI Number | 3013695852 |
Name | RESOUNDANT, INC. |
Owner & Operator | Resoundant, Inc. |
Contact Address | 421 1st Ave SW STE 204W Rochester MN 55902 US |
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 421 1st Ave SW STE 204W Rochester, MN 55902 US |
Establishment Type |
|
Device Company | Device | Date |
---|---|---|
RESOUNDANT, INC. | Flex Passive Driver Kit- Small | 2023-04-10 |
RESOUNDANT, INC. | Flex Passive Driver Kit- Large | 2023-04-10 |
RESOUNDANT, INC. | Passive Driver | 2023-03-01 |
RESOUNDANT, INC. | Hepatogram Plus MREPLUSV3 | 2022-04-21 |
RESOUNDANT, INC. | MREplus | 2021-04-09 |
RESOUNDANT, INC. | MREplus | 2021-04-09 |
Resoundant Inc | Resoundant Acoustic Driver System | 2020-07-10 |
RESOUNDANT, INC. | MREplus+ | 2019-08-21 |
Resoundant Inc | MREplus+ Software | 2019-08-01 |
RESOUNDANT, INC. | Resoundant | 2017-05-14 |