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Data / Medical devices / Knife, Ophthalmic / India

FDA-registered makers of Knife, Ophthalmic in India: 16 establishments

16 establishments in India are registered with the FDA to make Knife, Ophthalmic (product code HNN). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Knife, Ophthalmic
Product code
HNN
Country
India

Makers of Knife, Ophthalmic in India

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Akriti Ophthalmic Private LimitedHyderabad Telangana, IndiaManufacturer0000api.fda.gov
Appasamy Associates Private Limited ( Thruvandar Koil)Mannadipet Commune Puducherry, IndiaManufacturer0000api.fda.gov
Appasamy Associates Private Limited (MN Kuppam)Villupuram District Tamil Nadu, IndiaManufacturer0000api.fda.gov
AurolabMADURAI Tamil Nadu, IndiaContract manufacturer, Manufacturer0000api.fda.gov
Epsilon Eye Care Pvt., Ltd.MUMBAI Maharashtra, IndiaManufacturer0000api.fda.gov
Indo-German Surgical CorporationMumbai Maharashtra, IndiaExporter to the US, Manufacturer0000api.fda.gov
Iscon Surgicals, Ltd.JODHPUR Rajasthan, IndiaManufacturer0000api.fda.gov
Kdans Surgical Private LimitedGANDHINAGAR Gujarat, IndiaContract manufacturer0000api.fda.gov
M/S Tarun EnterprisesPrayagraj, Uttar Pradesh, IndiaManufacturer0000api.fda.gov
Madhu Instruments Pvt LtdNew Delhi, IndiaManufacturer0000api.fda.gov
Paramount Surgimed Ltd.BHIWADI Rajasthan, IndiaManufacturer0000api.fda.gov
Paul Instruments (india)CALCUTTA West Bengal, IndiaManufacturer0000api.fda.gov
Ribbel International Ltd.SONEPAT Haryana, IndiaManufacturer0000api.fda.gov
Shah Eye Care Private LimitedDAVANGERE Karnataka, IndiaManufacturer0000api.fda.gov
SpeedwayIndia Delhi, IndiaManufacturer0000api.fda.gov
Surgimed DevicesAHMEDABAD Gujarat, 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.