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Data / Medical devices / Airway, Oropharyngeal, Anesthesiology / India

FDA-registered makers of Airway, Oropharyngeal, Anesthesiology in India: 8 establishments

8 establishments in India are registered with the FDA to make Airway, Oropharyngeal, Anesthesiology (product code CAE). 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
Airway, Oropharyngeal, Anesthesiology
Product code
CAE
Country
India

Makers of Airway, Oropharyngeal, Anesthesiology in India

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Bio-Med Healthcare Products Pvt. Ltd.Palwal Haryana, IndiaContract manufacturer, Manufacturer0000api.fda.gov
Hospital Equipment MFG. Co.NOIDA Uttar Pradesh, IndiaManufacturer0000api.fda.gov
Harsoria Healthcare Pvt. Ltd. (Unit-2)Baddi Himachal Pradesh, IndiaContract manufacturer, Contract sterilizer0000api.fda.gov
Heuer International (A division of GST Corporation Limited)NOIDA Uttar Pradesh, IndiaForeign private label distributor, Manufacturer, Repackager or relabeler0000api.fda.gov
Lamed Private LimitedFARIDABAD Haryana, IndiaManufacturer0000api.fda.gov
Poly Medicure Ltd.Faridabad Haryana, IndiaManufacturer0000api.fda.gov
Romsons InternationalNOIDA Uttar Pradesh, IndiaManufacturer0000api.fda.gov
Suru International Pvt LtdDAHANU Maharashtra, IndiaManufacturer0000api.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.