FDA.reportPublic FDA data

MECTALENT LTD.

Matched from indexed company URL: MECTA Corporation

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30131561853013156185MECTALENT LTD.1N2026-01-01Veistamotie 15 Oulu Kainuu FI FI-90620
30205333020533MECTA Corporation1N2020-04-2519799 SW 95TH AVE SUITE B TUALATIN OR US 97062

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00861539000103spECTrum - 100 Joule ECT Device with 4 Parameter Setting Controls and Patient Monitoring(503) 612-6780info@mectacorp.com
00861539000110spECTrum - 100 Joule ECT Device with 1 Parameter Setting Control and Patient Monitoring(503) 612-6780info@mectacorp.com
00861539000127spECTrum - 100 Joule ECT Device with 4 Parameter Setting Controls(503) 612-6780info@mectacorp.com
00861539000134spECTrum - 100 Joule ECT Device with 1 Parameter Setting Control(503) 612-6780info@mectacorp.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
86201020620591K965070SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M.QGH1997-03-06
1958941166018024
86201822458315
1958941024765039
1958941094255519
1958941104402762
1958941176465636
1958941176726524
1958941184089838
1958941246106148
1958941327620566
1958941354524770
1958941399908711
1958941462908492
1958941471502761
1958941548134600
1958941593616358
1958941666610803
1958941674096307
1958941682584281
1958941687516618
1958941703232309
1958941768934870
1958941791527030
1958941801062130
1958941809754847
1958941842770235
1958941902916424

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
QGH11997-03-06

PMN#

GUDID#