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Data / Medical devices / India / Kashmir Surgical Works

Kashmir Surgical Works: FDA-registered device maker in AMBALA Haryana, India, 2 510(k) clearances

Kashmir Surgical Works is registered with the FDA (registration 3004765453) in AMBALA Haryana, India. It lists 19 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 10, 2006. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Kashmir Surgical Works
FDA registration number
3004765453
Address
1888-B/10 Baldev Nagar, AMBALA Haryana, India, 134007
Owner or operator
KASHMIR SURGICAL WORKS (10087074)
Roles
Exporter to the US, Manufacturer
First device listed
January 9, 2023
Registered through
2026
Brand names listed
Anaesthetic and respiratory equipment, BLOOD CELL COUNTER MANUAL 8 KEY, 5 KEY, Dental RVG, Denture Repair Kit, Diagnostic condensing lens., ESK CHARGER, Manual ophthalmic surgical instrument, OPHTHALMIC DISTANCE AND NEAR VISION WALL HANGING EYE CHART and more

Devices it lists

DeviceProduct codeClassRoleSource
Chart, Visual AcuityHOX1Exporter to the US, Manufactureraccessdata.fda.gov
Denture Repair KitEBO2Exporter to the US, Manufactureraccessdata.fda.gov
ExophthalmometerHLS1Exporter to the US, Manufactureraccessdata.fda.gov
Headlamp, Operating, Battery-OperatedHPP1Exporter to the US, Manufactureraccessdata.fda.gov
HemocytometerGHO1Exporter to the US, Manufactureraccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Exporter to the US, Manufactureraccessdata.fda.gov
Laryngoscope, RigidCCW1Exporter to the US, Manufactureraccessdata.fda.gov
Lens, Condensing, DiagnosticHJL1Exporter to the US, Manufactureraccessdata.fda.gov
Loupe, Binocular, Low PowerHJH1Exporter to the US, Manufactureraccessdata.fda.gov
Ophthalmoscope, Ac-PoweredHLI2Exporter to the US, Manufactureraccessdata.fda.gov
OtoscopeERA1Exporter to the US, Manufactureraccessdata.fda.gov
Research Use Only/PathologyOTUNExporter to the US, Manufactureraccessdata.fda.gov
Retinoscope, Ac-PoweredHKL2Exporter to the US, Manufactureraccessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)HOY1Exporter to the US, Manufactureraccessdata.fda.gov
Strip, SchirmerKYD1Exporter to the US, Manufactureraccessdata.fda.gov
System, Blood Collection, Vacuum-Assisted, ManualKST1Exporter to the US, Manufactureraccessdata.fda.gov
System, Image Processing, RadiologicalLLZ2Exporter to the US, Manufactureraccessdata.fda.gov
System, X-Ray, Extraoral Source, DigitalMUH2Exporter to the US, Manufactureraccessdata.fda.gov
Tester, Color VisionHIT1Exporter to the US, Manufactureraccessdata.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
March 10, 2006K060178VIX WIN PROMUHSubstantially EquivalentGendex Dental Systemsaccessdata.fda.gov
November 9, 1977K77190071110 DESK CHARGERHLSSubstantially EquivalentWelch Allyn, Inc.accessdata.fda.gov

Compare with other makers

Updated March 10, 2006. 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.