This page includes the latest FDA filings for Sq Products Ag. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3003403260 |
FEI Number | 3003403260 |
Name | SQ PRODUCTS AG |
Owner & Operator | SQ Products AG |
Contact Address | Industriestrasse 23 Inwil CH-LU Luzern 6034 CH |
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 | Industriestrasse 23 Inwil Luzern, 6034 CH |
Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
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SQ PRODUCTS AG | Univers Revers Modular Glenoid System | 2020-01-29 |
SQ PRODUCTS AG | Arthrex Eclipse Shoulder Prosthesis System | 2019-08-08 |
SQ PRODUCTS AG | Arthrex Eclipse Shoulder Prosthesis System | 2019-08-08 |
SQ PRODUCTS AG | Glenoid, Poly with Keel | 2019-02-14 |
SQ PRODUCTS AG | Glenoid, Poly with Keel | 2019-02-14 |
SQ PRODUCTS AG | Univers Revers Porous Coated Baseplate | 2018-11-13 |
SQ PRODUCTS AG | Univers Revers Porous Coated Baseplate | 2018-11-13 |
SQ PRODUCTS AG | Osteotome, Retractor, Elevator, Rasp, Broach | 2013-03-06 |
SQ PRODUCTS AG | Surgical Drill | 2013-03-06 |