Sq Products Ag

FDA Filings

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.

FDA Registration(s)
Registration Number3003403260
FEI Number3003403260
NameSQ PRODUCTS AG
Owner & OperatorSQ Products AG
Contact AddressIndustriestrasse 23
Inwil CH-LU Luzern 6034 CH
Official Correspondent
  • Matthias Hendel
  • 041-041-7485381-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressIndustriestrasse 23
Inwil Luzern, 6034 CH
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
SQ PRODUCTS AG
Univers Revers Modular Glenoid System2020-01-29
SQ PRODUCTS AG
Arthrex Eclipse Shoulder Prosthesis System2019-08-08
SQ PRODUCTS AG
Arthrex Eclipse Shoulder Prosthesis System2019-08-08
SQ PRODUCTS AG
Glenoid, Poly with Keel2019-02-14
SQ PRODUCTS AG
Glenoid, Poly with Keel2019-02-14
SQ PRODUCTS AG
Univers Revers Porous Coated Baseplate2018-11-13
SQ PRODUCTS AG
Univers Revers Porous Coated Baseplate2018-11-13
SQ PRODUCTS AG
Osteotome, Retractor, Elevator, Rasp, Broach2013-03-06
SQ PRODUCTS AG
Surgical Drill2013-03-06

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