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Data / Medical devices / Test, Luteinizing Hormone (Lh), Over The Counter / India

FDA-registered makers of Test, Luteinizing Hormone (Lh), Over The Counter in India: 7 establishments

7 establishments in India are registered with the FDA to make Test, Luteinizing Hormone (Lh), Over The Counter (product code NGE). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Test, Luteinizing Hormone (Lh), Over The Counter
Product code
NGE
Country
India

Makers of Test, Luteinizing Hormone (Lh), Over The Counter in India

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Biowick Healthcare Private LimitedBhopal Madhya Pradesh, IndiaContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Centum Electronics LimitedBangalore Karnataka, IndiaContract manufacturer0000api.fda.gov
Immunoscience India Pvt. Ltd.Pune Maharashtra, IndiaContract manufacturer, Exporter to the US0000api.fda.gov
Inito Health Tech Private LimitedBangalore, Bangalore South Karnataka, IndiaComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Mark EnterprisesNashik Maharashtra, IndiaManufacturer0000api.fda.gov
Meril Diagnostics Pvt. Ltd.Vapi Gujarat, IndiaManufacturer0000api.fda.gov
Ubio Biotechnology Systems Pvt.LtdKalamassery Kerala, IndiaContract manufacturer, Exporter to the US0000api.fda.gov

Updated November 2, 2026. 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.