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Data / Medical devices / India / Latrile Gloves Private Limited

Latrile Gloves Private Limited: FDA-registered device maker in DINDIGUL Tamil Nadu, India, 1 510(k) clearance

Latrile Gloves Private Limited is registered with the FDA (registration 3033527714) in DINDIGUL Tamil Nadu, India. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 28, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3033527714
Address
Plot No: B5 - Sipcot Induatrial Complex, 8TH Main Road Pallapatti Village, Nilakottai Taluk, DINDIGUL Tamil Nadu, India, 624201
Owner or operator
LATRILE GLOVES PRIVATE LIMITED (10091525)
Roles
Manufacturer
First device listed
October 11, 2024
Registered through
2026
Brand names listed
Blue Nitrile Examination Gloves Powder Free

Devices it lists

DeviceProduct codeClassRoleSource
Polymer Patient Examination GloveLZA1Manufactureraccessdata.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
May 28, 2023K230601Blue Nitrile Examination Gloves Powder FreeLZASubstantially EquivalentLatrile Gloves Private Limitedaccessdata.fda.gov

Compare with other makers

Updated May 28, 2023. 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.