Ohlendorf Co

FDA Filings

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

FDA Registration(s)
Registration Number1000380364
FEI Number1000380364
NameOHLENDORF COMPANY
Owner & OperatorOHLENDORF COMPANY
Contact Address2840 CLARK AVENUE --
Saint Louis MO 63103 US
Official Correspondent
  • Kevin M OHLENDORF
  • x-314-5333440-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2840 CLARK AVENUE
ST. LOUIS, MO 63103 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
OHLENDORF COMPANY
Perio Protect Tray2006-04-27

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