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 |
|---|---|---|
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 |