Kitotech Medical Inc

FDA Filings

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

FDA Registration(s)
Registration Number3012261738
FEI Number3012261738
NameKITOTECH MEDICAL INC
Owner & OperatorKitoTech Medical Inc
Contact Address500 Yale Ave N
Seattle WA 98109 US
Official Correspondent
  • Ronald Berenson
  • 1-206-7901094-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address500 Yale Ave N
Seattle, WA 98109 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Kitotech Medical Inc
microMend PRO MM01SU22024-05-17
Kitotech Medical Inc
microMend PRO MM12LG42024-05-17
Kitotech Medical Inc
microMend MSXWD0042024-05-17
Kitotech Medical Inc
microMend M2SXD0022024-05-17
Kitotech Medical Inc
microMend PRO MM01XS22024-05-17
Kitotech Medical Inc
microMend PRO MM01W2A2024-05-17
Kitotech Medical Inc
microMend PRO MM01W2S2024-05-17
Kitotech Medical Inc
microMend PRO MM12SM42024-05-17
Kitotech Medical Inc
microMend PRO MM01LG22024-05-17
Kitotech Medical Inc
microMend PRO MM12XS22024-05-17
Kitotech Medical Inc
microMend M3S2D0012024-05-17
Kitotech Medical Inc
microMend PRO MM01SM22024-05-17
Kitotech Medical Inc
BackVive P2B1D0012024-05-06
Kitotech Medical Inc
microMend M1S2K0032023-09-26
Kitotech Medical Inc
microMend M1L2K0052023-09-25
Kitotech Medical Inc
microMend M1S2K0012023-09-25
Kitotech Medical Inc
microMend M1L2K0062023-03-08
KITOTECH MEDICAL INC
microMend2016-02-17
KITOTECH MEDICAL INC
microMend2016-02-17

Related Finance Registrations

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.