Organon Teknika Corp L L C

FDA Filings

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

FDA Registration(s)
Registration Number1039284
FEI Number1039284
NameOrganon Teknika Corporation LLC
Owner & OperatorMerck Sharp and Dohme Corp.
Contact Address1180 Church Road - Suite 1
Lansdale PA 19446 US
Official Correspondent
  • Foram S Devdhara
  • x-215-6315131-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address100 Rodolphe Street Building 1300
Durham, NC 27712 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Merck Sharp & Dohme Corp., Merck Teknika LLC
Other Medication2023-12-08
Merck Sharp & Dohme Corp., Merck Teknika LLC
Other Medication2022-09-23
Merck Sharp & Dohme Corp., Merck Teknika LLC
Other Medication2022-09-14
Merck Sharp & Dohme Corp., Merck Teknika LLC
Other Medication2022-06-17
Merck Sharp & Dohme Corp., Merck Teknika LLC
Other Medication2021-06-08
Merck Sharp & Dohme Corp., Merck Teknika LLC
Other Medication2021-02-06
Merck Sharp & Dohme Corp., Merck Teknika LLC
Other Medication2020-09-16
Merck Sharp & Dohme Corp., Merck Teknika LLC
Other Medication2019-09-19
Organon Teknika Corporation LLC [Merck Sharp and Dohme Corp.]
BCG Vaccine (multiple puncture device)2018-05-22

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