This page includes the latest FDA filings for Danette Wilson. 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 |
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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 |