Devicor Medical Products Inc Warehouse Distribution Center

FDA Filings

This page includes the latest FDA filings for Devicor Medical Products Inc Warehouse Distribution Center. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3010339638
FEI Number3010339638
NameDevicor Medical Products, Inc. Warehouse/Distribution Center
Owner & OperatorDevicor Medical Products, Inc.
Contact Address300 E-Business Way Fifth Floor
Cincinnati OH 45241 US
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address4750 Lake Forest Dr Ste 120
Blue Ash, OH 45242 US
Establishment Type
  • Manufacture Medical Device
  • Remanufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.]
Sentimag2016-12-05
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.]
CoreVISION Digital Specimen Radiography (DSR) System2016-12-05
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.]
HydroMark2016-06-27
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.]
HydroMark2016-06-27
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.]
HydroMark2016-06-10
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.]
Mammotome revolve2016-03-16
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.]
Mammotome? Hand Held System2010-07-30
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.]
Mammotome? MR Biopsy System2010-07-30
Devicor Medical Products, Inc. Warehouse/Distribution Center [Devicor Medical Products, Inc.]
Mammotome? EX Hand Held System2010-07-30

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