Scanlan Group Logistics Center

FDA Filings

This page includes the latest FDA filings for Scanlan Group Logistics Center. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3013424760
FEI Number3013424760
NameScanlan Group Logistics Center
Owner & OperatorSURGICAL TECHNOLOGIES, INC.
Contact Address292 EAST LAFAYETTE FRONTAGE RD --
Saint Paul MN 55107 US
Official Correspondent
  • Waylon C Vanderpoel
  • x-651-2279953-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address285 Florida Street
Saint Paul, MN 55107 US
Establishment Type
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Repack or Relabel Medical Device

FDA Filings

Device
Company
DeviceDate
Scanlan Group Logistics Center [SURGICAL TECHNOLOGIES, INC.]
SCANLAN? Thoracoscopic Scissors2017-09-19
Scanlan Group Logistics Center [SURGICAL TECHNOLOGIES, INC.]
SCANLAN? Thoracoscopic Needle Holder2017-09-19
Scanlan Group Logistics Center [SURGICAL TECHNOLOGIES, INC.]
SCANLAN? Thoracoscopic Clamp2017-09-19
Scanlan Group Logistics Center [SURGICAL TECHNOLOGIES, INC.]
MiStent SES? Sirolimus Eluting Absorbable Polymer Coronary Stent System2015-08-26

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