This page includes the latest FDA filings for Schoepf Fertigungstechnik 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 | 3015131021 |
FEI Number | 3015131021 |
Name | SCHOEPF FERTIGUNGSTECHNIK GMBH |
Owner & Operator | SCHOEPF Fertigungstechnik GmbH |
Contact Address | Hauptstrasse 65 Bludesch AT-8 Vorarlberg 6719 AT |
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 | Hauptstrasse 65 Bludesch Vorarlberg, 6719 AT |
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
---|---|---|
SCHOEPF FERTIGUNGSTECHNIK GMBH | Articulator CA 3.0 | 2018-12-17 |
SCHOEPF FERTIGUNGSTECHNIK GMBH | Universal Transferbow | 2018-12-12 |
SCHOEPF FERTIGUNGSTECHNIK GMBH | Universal Transferbow System (UTS) | 2018-12-12 |
SCHOEPF FERTIGUNGSTECHNIK GMBH | Clinical Instrument Set | 2018-12-12 |
SCHOEPF FERTIGUNGSTECHNIK GMBH | CRS Set 20 | 2018-12-12 |
SCHOEPF FERTIGUNGSTECHNIK GMBH | CRS Set 15 | 2018-12-12 |
SCHOEPF FERTIGUNGSTECHNIK GMBH | CRS Set 10 | 2018-12-12 |