Matrix Surgical Usa

FDA Filings

This page includes the latest FDA filings for Matrix Surgical Usa. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3009383407
FEI Number3009383407
NameMATRIX SURGICAL USA
Owner & OperatorMatrix Surgical USA
Contact Address4025 Welcome All Road Suite 120
Atlanta GA 30349 US
Official Correspondent
  • John T O'Shaughnessy
  • 1-404-8554592-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address4025 WELCOME ALL RD SW SUITE 120
Atlanta, GA 30349 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
MATRIX SURGICAL USA
OMNIPORE DUROMAX ZB Orbital Implant2018-11-17
MATRIX SURGICAL USA
OMNIPORE DUROMAX Surgical Implants2018-11-17
MATRIX SURGICAL USA
OmniPore Customized Surgical Implant2014-06-16
MATRIX SURGICAL USA
HTR-OMNIPORE Patient Matched Implant2014-06-16
MATRIX SURGICAL USA
OMNIPORE(R) Surgical Implant2013-08-06
MATRIX SURGICAL USA
OMNIPORE SURGICAL IMPLANTS AND ACCESSORIES2013-07-31

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