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Data / Medical devices / South Korea / Vpix Medical, Inc.

Vpix Medical, Inc.: FDA-registered device maker in Jung-gu Daejeon, South Korea, 2 510(k) clearances

Vpix Medical, Inc. is registered with the FDA (registration 3021744379) in Jung-gu Daejeon, South Korea. It lists 7 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 13, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3021744379
Address
774, Gyeryong-ro, Jung-gu Daejeon, South Korea, 34873
Owner or operator
VPIX Medical, Inc. (10084429)
Roles
Manufacturer
First device listed
February 21, 2022
Registered through
2026
Brand names listed
Topi - FNa, Topi - ICG, VPIX Viewer, cCeLL - Ex vivo(Models: CX100-2W2C488775, CX100-1W1C405, CX100-1W1C488, CX100-1W1C775), cCeLL - In vivo, cCeLL - In vivo with Drop-In Robo

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
February 13, 2026K251852cCeLL - In vivo with Drop-In Robo (CN100-2W2C488775, CN100-1W1C775, DR200)OWNSubstantially EquivalentVPIX Medical, Inc.accessdata.fda.gov
August 21, 2024K233391cCeLL - In vivoGWGSubstantially EquivalentVPIX Medical, Inc.accessdata.fda.gov

Compare with other makers

Updated February 13, 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.