510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K211326Substantially Equivalent

EndoScreener

Chengdu Wision Medical Device Co., Ltd., Chengdu, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K211326 is the FDA 510(k) clearance record for EndoScreener, a class II device, cleared for Chengdu Wision Medical Device Co., Ltd. on under FDA product code QNP (Gastrointesinal Lesion Software Detection System). FDA's definition for product code QNP reads: "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...". FDA records list one 510(k) clearance for Chengdu Wision Medical Device Co., Ltd. As of , FDA records show no recalls naming K211326.

Clearance record

Decision date
Received
(203 days to decision)
Product code
QNP Gastrointesinal Lesion Software Detection System
Regulation
21 CFR 876.1520
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Chengdu Wision Medical Device Co., Ltd. Unit 802, Floor 8, Bldg. 17, Yintaicheng, # 1999 Yizhou, Chengdu, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QNP

Trailing 12 months
6 clearances under product code QNP in the twelve months to October 2026, August 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code QNP, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20261
May 20261
June 20260
July 20260
August 20262
September 20261
October 20260