This page includes the latest FDA filings for Reapplix. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3014326253 |
FEI Number | 3014326253 |
Name | Christy Foreman |
Owner & Operator | Reapplix |
Contact Address | Blokken 45 Birker?d DK-85 Region Sjaelland 3460 DK |
Official Correspondent |
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US Agent |
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Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 1555 King Street, Suite 300 Alexandria, VA 22314 US |
Establishment Type | Manufacture Medical Device |
Registration Number | 3014635672 |
FEI Number | 3014635672 |
Name | Reapplix US |
Owner & Operator | Reapplix |
Contact Address | Blokken 45 Birker?d DK-85 Region Sjaelland 3460 DK |
Official Correspondent |
|
Registration Status | 1 |
Initial Importer | Y |
Registration Expiration | 2020-04-25 |
Registration Address | 325 Miron Drive, Suite 140 Southlake, TX 76092 US |
Device Company | Device | Date |
---|---|---|
Christy Foreman [Reapplix] | 3CP Counterbalance | 2018-03-01 |
Christy Foreman [Reapplix] | 3CP Centrifuge | 2018-03-01 |
Christy Foreman [Reapplix] | 3C Patch System | 2018-03-01 |
Christy Foreman [Reapplix] | 3C Patch System | 2018-03-01 |
Christy Foreman [Reapplix] | 3C Patch Needle Holder | 2018-03-01 |
Christy Foreman [Reapplix] | 3C Patch Kit | 2018-03-01 |
Christy Foreman [Reapplix] | 3C Patch Device | 2018-03-01 |