Mecta Corp

FDA Filings

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

FDA Registration(s)
Registration Number3020533
FEI Number3020533
NameMECTA Corporation
Owner & OperatorMECTA Corporation
Contact Address19799 SW 95TH AVE SUITE B --
Tualatin OR 97062 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address19799 SW 95TH AVE SUITE B
TUALATIN, OR 97062 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Device in the United States for Export Only



FDA Filings

Device
Company
DeviceDate
Mecta Corporation
MECTA Sigma2020-04-26
MECTA CORPORATION
spECTrum 2018-07-06
MECTA CORPORATION
spECTrum 2018-07-06
MECTA CORPORATION
spECTrum 2018-07-06
MECTA CORPORATION
spECTrum 2018-07-06
MECTA Corporation
MECTA spECTrum 200J2015-07-07
MECTA Corporation
MECTA spECTrum2008-01-17
MECTA CORP.
SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M.1997-03-06
MECTA CORP.
SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 M1996-09-18
MECTA CORP.
MECTA ECT DEVICE MODELS SR & JR1985-08-09

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