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Qpix Solutions, Inc. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Qpix Solutions, Inc. has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Qpix Solutions, Inc." is on file.

What these totals cover: FDA records filed under the name "Qpix Solutions, Inc." and its spelling variant "Qpix Solutions".

Latest 510(k): Sep 30, 2026

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	4	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	0	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

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Recent 510(k) clearances

4 510(k) clearances from Sep 27, 2023 to Sep 30, 2026.

K-Number	Device	Date
K261663	EzSensor HD	Sep 30, 2026
K252570	EzSensor HD, EzSensor UHD	Nov 10, 2025
K242778	X Sensor (Model: IOS-A15IF, HDI-15DGF)	Oct 11, 2024
K232255	EZSensor XHD	Sep 27, 2023

Qpix Solutions, Inc. and the FDA: common questions

Has Qpix Solutions, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "Qpix Solutions, Inc." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Qpix Solutions, Inc. received an FDA Form 483?

FDA has not published a Form 483 for "Qpix Solutions, Inc." in its reading room. FDA publishes some Form 483s, not all of them.

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