Renovo Inc

FDA Filings

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

FDA Registration(s)
Registration Number3014023545
FEI Number3014023545
NameRENOVO, INC.
Owner & OperatorReNovo, Inc
Contact Address340 SW Columbia St
Bend OR 97702 US
Official Correspondent
  • Mark Wells
  • x-541-4228880-110
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address340 SW COLUMBIA ST
Bend, OR 97702 US
Establishment TypeReprocess Single-Use Device

FDA Owner/Operator Registration

FDA Filings

Device
Company
DeviceDate
ReNovo, Inc.
Reprocessed DePuy Mitek Ablation Wand2018-03-19
ReNovo, Inc.
Reprocessed ArthoCare Ablation Wand2018-03-05
ReNovo, Inc.
Reprocessed ArthroCare ENT Coblator2018-02-21
Renovo, Inc.
Reprocessed Ethicon Bladeless Trocars; Reprocessed Ethicon Universal Trocar Sleeves2017-10-06
Renovo, Inc.
Reprocessed Covidien Trocar2017-10-05
Renovo, Inc.
Reprocessed Shavers/Burs2017-10-04

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Related Finance Registrations
SEC0001661397ReNovo, Inc. of OREGON
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