Meditec Devices

FDA Filings

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

FDA Registration(s)
Registration Number3006389770
FEI Number3006389770
NameMEDITEC DEVICES
Owner & OperatorMEDITEC DEVICES
Contact AddressB-3, AJANTA, OPP.KAMAT CLUB, S.V.ROAD, GOREGAON WEST,
MUMBAI, MAHARASHTRA IN-NOTA 400062 IN
Official Correspondent
  • SAJJAN - PAUL
  • 91-22-28722523-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2A MITUL IND. ESTATE, SATIVALI ROAD,
VASAI(E), THANE, MAHARASHTRA Maharashtra, 401208 IN
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
MEDITEC DEVICES
Remover Intrauterine Device Hook Type2020-02-05
MEDITEC DEVICES
NA2017-02-27
MEDITEC DEVICES
Uterine Sound2016-07-19
MEDITEC DEVICES
Safety Scalpel2016-02-24
MEDITEC DEVICES
Target Point2015-07-16
MEDITEC DEVICES
Earwell2013-03-11
MEDITEC DEVICES
Robertazzi2013-03-11
MEDITEC DEVICES
Soft Dilators2011-03-14
MEDITEC DEVICES
Dennis Dilators2011-03-14
MEDITEC DEVICES
Phem Alert2011-01-21
MEDITEC DEVICES
COMFORT FIT MONASCOPE2007-01-29
MEDITEC DEVICES
Ported Introducer2007-01-05
MEDITEC DEVICES
Malleable Introducer2007-01-05
MEDITEC DEVICES
ET Introducer2007-01-05
MEDITEC DEVICES
Coated Stylet2007-01-05
MEDITEC DEVICES
Aluminium Stylet2007-01-05