Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Dual Core

K-Number: K260805 · 2026-05-11

ApplicantVericom Co., Ltd.
Decision Date2026-05-11
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Dual Core is a medical device manufactured by Vericom Co., Ltd.. It received FDA 510(k) clearance on 2026-05-11 under approval number K260805. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dual Core?

Dual Core is a medical device that received FDA 510(k) clearance on 2026-05-11. It is manufactured by Vericom Co., Ltd.. The 510(k) number is K260805.

When was Dual Core approved by the FDA?

Dual Core received FDA 510(k) clearance on 2026-05-11, under approval number K260805.

What company makes Dual Core?

Dual Core is manufactured by Vericom Co., Ltd..

What is the FDA product code for Dual Core?

The FDA product code for Dual Core is EBF.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑