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Data / Medical devices / India / Liberty Med Supplies Pvt Ltd

Liberty Med Supplies Pvt Ltd: FDA-registered device maker in KOTTAYAM Kerala, India, 1 510(k) clearance

Liberty Med Supplies Pvt Ltd is registered with the FDA (registration 3021192208) in KOTTAYAM Kerala, India. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 8, 2018. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3021192208
Address
Ezhacherry P O, Ramapuram, KOTTAYAM Kerala, India, 686651
Owner or operator
LIBERTY MED SUPPLIES PVT LTD (10083709)
Roles
Manufacturer
First device listed
December 13, 2021
Registered through
2026
Brand names listed
PRISTEEN, Protezione

Devices it lists

DeviceProduct codeClassRoleSource
Latex Patient Examination GloveLYY1Manufactureraccessdata.fda.gov
Surgeon'S GlovesKGO1Manufactureraccessdata.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
January 8, 2018K172942Pristeen (Latex Surgeon’s Gloves Powder Free, Polymer coated with protein content labeling claim of 50 ug/dm2 or less per glove of extractable proteinKGOSubstantially EquivalentBeta Healthcare Products Pvt., Ltd.accessdata.fda.gov

Compare with other makers

Updated January 8, 2018. 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.