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Data / Medical devices / India / Appasamy Associates Private Limited ( Ambattur)

Appasamy Associates Private Limited ( Ambattur): FDA-registered device maker in Chennai Tamil Nadu, India, 2 510(k) clearances

Appasamy Associates Private Limited ( Ambattur) is registered with the FDA (registration 3010675798) in Chennai Tamil Nadu, India. It lists 13 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 9, 2011. Registered through 2026. 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.

Get makers like this oneWatch Appasamy Associates Private Limited ( Ambattur)
FDA registration number
3010675798
Address
Appasamy Associates Private Limited 446 Sidco Industrial Estate, Ambattur, Chennai Tamil Nadu, India, 600098
Owner or operator
Appasamy Associates Private Limited (10052771)
Roles
Manufacturer
First device listed
October 5, 2016
Registered through
2026
Brand names listed
Appa Keratoscope, Appa chair Ophthalmic, Appasamy -Chair Ophthalmic Manual, Appasamy Lens Meaduring Instrument- Lensometer, Appasamy Microscope, Non-Electric ,Ophthalmic, Appasamy Ophthalmoscope Ac-powered, Appasamy Ophthalmoscope, Battery-Powered, Appasamy Refractor Manual-Refractor ,Manual, nonPowered and more

Devices it lists

DeviceProduct codeClassRoleSource
Biomicroscope, Slit-Lamp, Ac-PoweredHJO2Manufactureraccessdata.fda.gov
Chair, Examination And TreatmentFRK1Manufactureraccessdata.fda.gov
Chair, Ophthalmic, Ac-PoweredHME1Manufactureraccessdata.fda.gov
Chair, Ophthalmic, ManualHMD1Manufactureraccessdata.fda.gov
Instrument, Measuring, Lens, Ac-PoweredHLM1Manufactureraccessdata.fda.gov
Keratoscope, Ac-PoweredHLQ1Manufactureraccessdata.fda.gov
Keratoscope, Battery-PoweredHLR1Manufactureraccessdata.fda.gov
Microscope, Operating, Non-Electric, OphthalmicHRB1Manufactureraccessdata.fda.gov
Ophthalmoscope, Ac-PoweredHLI2Manufactureraccessdata.fda.gov
Ophthalmoscope, Battery-PoweredHLJ2Manufactureraccessdata.fda.gov
Refractor, Manual, Non-Powered, Including PhoropterHKN1Manufactureraccessdata.fda.gov
Stand, Instrument, Ophthalmic, Non-PoweredHMG1Manufactureraccessdata.fda.gov
Table, Instrument, Manual, OphthalmicHRK1Manufactureraccessdata.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
February 9, 2011K110205AAIO-7, AAIO WIRLESSHLISubstantially EquivalentAppasamy Associatesaccessdata.fda.gov
July 31, 2008K082031APPASAMY SLIT LAMP, A1A-11 AND A1A-12 SERIESHJOSubstantially EquivalentAppasamy Associatesaccessdata.fda.gov

Compare with other makers

Updated February 9, 2011. 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.