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FDA PRODUCT CODE · CLASS II

QNPGastrointesinal Lesion Software Detection System

A gastrointestinal lesion software detection system is a computer-assisted detection device used in conjunction with endoscopy for the detection of abnormal lesions in the gastrointestinal tract. This device with advanced software algorithms brings attention to images to aid in the detection of lesions. The device may contain hardware to support interfacing with an endoscope.

DEVICE CLASS
Class II
REGULATION
21 CFR 876.1520
MEDICAL SPECIALTY
Gastroenterology, Urology
REVIEW PANEL
GU
ImplantLife-sustainingGMP-exemptThird-party review eligible
7
510(K)/PMA CLEARANCES
510k: 7
0
RECALL ENTRIES

Recent clearances

K261369Cosmo Artificial Intelligence - Ai, Ltd. · 510k2026-05-29
K260724Magentiq Eye, Ltd. · 510k2026-04-03
K253664Iterative Health · 510k2025-12-22
K252178Magentiq Eye, Ltd. · 510k2025-10-03
K252586Odin Medical Limited · 510k2025-09-12
K251126Iterative Health · 510k2025-05-09
K244023Magentiq Eye, Ltd. · 510k2025-01-24

Related on SPEQ

Medical devices industryMedical device quality (ISO 13485)FDA device clearancesFDA enforcement & recalls

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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