MAGENTIQ-COLO (ME-APDS)
K-Number: K260724 · 2026-04-03
Device Summary
Frequently Asked Questions
What is the MAGENTIQ-COLO (ME-APDS)?
MAGENTIQ-COLO (ME-APDS) is a medical device that received FDA 510(k) clearance on 2026-04-03. The listed applicant is Magentiq Eye, Ltd.. The 510(k) number is K260724.
When did MAGENTIQ-COLO (ME-APDS) receive FDA 510(k) clearance?
MAGENTIQ-COLO (ME-APDS) received FDA 510(k) clearance on 2026-04-03, under 510(k) number K260724.
Who is the listed applicant for MAGENTIQ-COLO (ME-APDS)?
The FDA 510(k) record lists Magentiq Eye, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAGENTIQ-COLO (ME-APDS)?
The FDA product code for MAGENTIQ-COLO (ME-APDS) is QNP.
Other records listing Magentiq Eye, Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: QNP)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.