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Data / Medical devices / India / Innaccel Technologies Private Limited

Innaccel Technologies Private Limited: FDA-registered device maker in BANGALORE Karnataka, India, 1 510(k) clearance

Innaccel Technologies Private Limited is registered with the FDA (registration 3013345545) in BANGALORE Karnataka, India. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 6, 2026. 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.

FDA registration number
3013345545
Address
4, 5TH Floor, Aanand Towers, Raja Rammohan Roy Road Near Richmond Circle,sampangiramanagar, BANGALORE Karnataka, India, 560025
Owner or operator
INNACCEL TECHNOLOGIES PRIVATE LIMITED (10060033)
Roles
Manufacturer, Specification developer
First device listed
March 22, 2019
Registered through
2026
Brand names listed
Saans (F4-01-00-000-000), Saans Air Blender for CPAP, HFNC and Resuscitation, Saans Helmet, Saans pressure controller for CPAP, HFNC and Resuscitation, VAPCare, VAPLumen

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
January 6, 2026K251165Saans (F4-01-00-000-000)SGRSubstantially EquivalentInnaccel Technologies Private Limitedaccessdata.fda.gov

Compare with other makers

Updated January 6, 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.