This page includes the latest FDA filings for Rynel Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 1225263 |
| FEI Number | 3000719717 |
| Name | Rynel Inc. |
| Owner & Operator | MOLNLYCKE HEALTH CARE US LLC |
| Contact Address | 5550 Peachtree Parkway, Suite 500 Norcross GA 30092 US |
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 11 Twin Rivers Drive Wiscasset, ME 04578 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
Rynel Inc. [MOLNLYCKE HEALTH CARE US LLC] | E-Z Derm | 2013-01-08 |
Rynel Inc. [MOLNLYCKE HEALTH CARE US LLC] | Tubipad | 2009-02-06 |
Rynel Inc. [MOLNLYCKE HEALTH CARE US LLC] | Tubigrip | 2009-02-06 |
Rynel Inc. [MOLNLYCKE HEALTH CARE US LLC] | Tubifast | 2009-02-06 |
Rynel Inc. [MOLNLYCKE HEALTH CARE US LLC] | Setopress | 2009-02-06 |
Rynel Inc. [MOLNLYCKE HEALTH CARE US LLC] | Dermafit | 2009-02-06 |