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Remidio Innovative Solutions Private Limited: FDA-registered device maker in Bengaluru Karnataka, India, 1 510(k) clearance

Remidio Innovative Solutions Private Limited is registered with the FDA (registration 3013158193) in Bengaluru Karnataka, India. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 12, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3013158193
Address
No, 1 51 2/12 Vacuum technologies Compound Peenya 1st stage, Bengaluru Karnataka, India, 560058
Owner or operator
Remidio Innovative Solutions Private Limited (10052212)
Roles
Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed
June 29, 2016
Registered through
2026
Brand names listed
Anterior Imaging Module (AIM), C3 Field Analyzer (C3FA), Fundus On Phone Non Mydriatic (FOP NM-10), Fundus on Phone Non Mydriatic, InstaFOP16, InstaPSL16, InstaVue, InstaZ (Automated Fundus Camera) and more

Devices it lists

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
December 12, 2025K252120Fundus On Phone Non Mydriatic (FOP NM-10)HKISubstantially EquivalentRemidio Innovative Solutions Private Limitedaccessdata.fda.gov

Compare with other makers

Updated December 12, 2025. 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.