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Data / Medical devices / India / Mankind Pharma Limited

Mankind Pharma Limited: FDA-registered device maker in Paonta Sahib, Sirmaur Himachal Pradesh, India, 1 510(k) clearance

Mankind Pharma Limited is registered with the FDA (registration 3009083745) in Paonta Sahib, Sirmaur Himachal Pradesh, India. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 10, 2024. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3009083745
Address
Unit-III, Village Kunja Rampur Ghat Road, Opp. Dental College, Paonta Sahib, Sirmaur Himachal Pradesh, India, 173025
Owner or operator
Mankind Pharma Limited (10090583)
Roles
Manufacturer
First device listed
April 16, 2024
Registered through
2027
Brand names listed
Sodium Chloride Inhalation Solution, USP, 0.9%, 3% and 7%

Devices it lists

DeviceProduct codeClassRoleSource
Nebulizer (Direct Patient Interface)CAF2Manufactureraccessdata.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
April 10, 2024K232523Sodium Chloride Inhalation Solution, USP 0.9%, 3% & 7%CAFSubstantially EquivalentMankind Pharma Limitedaccessdata.fda.gov

Compare with other makers

Updated April 10, 2024. 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.