This page includes the latest FDA filings for Klingel Medical Metal G M B H. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3004370612 |
FEI Number | 3004370612 |
Name | Franz Menean |
Owner & Operator | Klingel medical metal GmbH |
Contact Address | Hanauer Str. 5-7 Pforzheim DE-BW Baden-Wurttemberg 75181 DE |
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 | 112 CORPORATE DR Portsmouth, NH 03801 US |
Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
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Franz Menean [Klingel medical metal GmbH] | Titanium scan body | 2012-11-26 |
Franz Menean [Klingel medical metal GmbH] | Titanium Base | 2011-04-04 |