Anil Dhingra

FDA Filings

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

FDA Registration(s)
Registration Number3002807616
FEI Number3002807616
NameANIL DHINGRA
Owner & OperatorMEDISPEC, LTD.
Contact Address40 HATAASIYA ST. P.O. BOX 292
YEHUD IL-NOTA 5610103 IL
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address203 Perry Pkwy Ste 6
Gaithersburg, MD 20877 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
ANIL DHINGRA [MEDISPEC, LTD.]
ECONOLITH Model 2000 Lithotripter System2010-11-22
ANIL DHINGRA [MEDISPEC, LTD.]
Lithospec2009-04-14
ANIL DHINGRA [MEDISPEC, LTD.]
Orthospec2007-12-07
ANIL DHINGRA [MEDISPEC, LTD.]
SlimSpec2006-12-19
ANIL DHINGRA [MEDISPEC, LTD.]
RADIALSPEC2006-12-19
ANIL DHINGRA [MEDISPEC, LTD.]
ED10002006-12-19
ANIL DHINGRA [MEDISPEC, LTD.]
Contour Wave2006-12-19
ANIL DHINGRA [MEDISPEC, LTD.]
Econolith EM10002005-07-18
ANIL DHINGRA [MEDISPEC, LTD.]
Econolith E30002005-07-18
ANIL DHINGRA [MEDISPEC, LTD.]
Urospec2005-07-18

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