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Data / Medical devices / India / Global Medikit Limited

Global Medikit Limited: FDA-registered device maker in Dehradun Uttarakhand, India, 1 510(k) clearance

Global Medikit Limited is registered with the FDA (registration 3040339315) in Dehradun Uttarakhand, India. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 29, 2022. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3040339315
Address
Khasra No. 323 (MI), Central Hope Town, Camp Road, Selaqui, Dehradun Uttarakhand, India, 248197
Owner or operator
Global Medikit Limited (10093948)
Roles
Complaint file establishment, Manufacturer
First device listed
August 18, 2025
Registered through
2026
Brand names listed
Glospine, HMG spinal Needle

Devices it lists

DeviceProduct codeClassRoleSource
Needle, Conduction, Anesthetic (W/Wo Introducer)BSP2Complaint file establishment, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
July 29, 2022K212982Medispine - Spinal Needle, Glospine - Spinal NeedleBSPSubstantially EquivalentGlobal Medikit Limitedaccessdata.fda.gov

Compare with other makers

Updated July 29, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.