This page includes the latest FDA filings for Dune Medical Devices L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3005755031 | ||||||
| FEI Number | 3005755031 | ||||||
| Name | Danette Wilson | ||||||
| Owner & Operator | Dune Medical Devices Ltd. | ||||||
| Contact Address | 6120 Windward Parkway Suite 160 Alpharetta GA 30005 US | ||||||
| Official Correspondent |
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| US Agent |
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| Importing Logistics Registration |
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| Registration Status | 1 | ||||||
| Initial Importer | N | ||||||
| Registration Expiration | 2020-04-25 | ||||||
| Registration Address | 6120 Windward Parkway Suite 160 Alpharetta, GA 30005 US | ||||||
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
| DUNE MEDICAL DEVICES LTD | MarginProbe® Probe | 2018-07-06 |
Danette Wilson [Dune Medical Devices Ltd.] | MarginProbe System | 2013-01-08 |
Danette Wilson [Dune Medical Devices Ltd.] | MarginProbe Probe | 2013-01-08 |
Danette Wilson [Dune Medical Devices Ltd.] | MarginProbe Console | 2013-01-08 |
| NCAGE Code | 4447A | DUNE MEDICAL DEVICES LTD |
| CAGE Code | 4447A | DUNE MEDICAL DEVICES LTD |