T K India Pvt L T D

FDA Filings

This page includes the latest FDA filings for T K India Pvt L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3013515223
FEI Number3013515223
NameT.K. India Pvt. Ltd.
Owner & OperatorTeleflex
Contact Address3015 Carrington Mill Blvd.
Morrisville NC 27560 US
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressPlot No. 346-347 Industrial Area Phase 2
Chandigarh Chandigarh, 160 002 IN
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
T.K. India Pvt. Ltd. [Teleflex]
Rusch MRI2017-02-27
T.K. India Pvt. Ltd. [Teleflex]
TruLite Secure2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
TruLED2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
Standard Laryngoscope Blades and Handles2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
SnapLight2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
Shucman 22005-03-03
T.K. India Pvt. Ltd. [Teleflex]
Rusch Polaris2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
Rusch LiteSlim2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
Rusch GreenLite2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
GreenSpec2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
GreenLED2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
Fiber Optic Laryngoscope Blades and Handles2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
EquipLite2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
EquipLED2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
Dolphin2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
DispoLED2005-03-03
T.K. India Pvt. Ltd. [Teleflex]
DispoGrip2005-03-03

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