This page includes the latest FDA filings for Gynesonics. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3005875675 |
| FEI Number | 3005875675 |
| Name | GYNESONICS, INC. |
| Owner & Operator | Gynesonics |
| Contact Address | 600 Chesapeake Drive Redwood City CA 94063 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 600 Chesapeake Drive REDWOOD CITY, CA 94063 US |
| Establishment Type | Develop Specifications But Do Not Manufacture At This Facility |
Device Company | Device | Date |
|---|---|---|
GYNESONICS, INC. [Gynesonics] | Sonata? Sonography-Guided Transcervical Fibroid Ablation System | 2018-09-18 |
GYNESONICS, INC. [Gynesonics] | Sonata? Sonography-Guided Transcervical Fibroid Ablation System | 2018-09-18 |
GYNESONICS, INC. [Gynesonics] | Sonata? Sonography-Guided Transcervical Fibroid Ablation System | 2018-09-18 |