ClearanceBrief
Company ยท TW

Visgeneer, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2006 to 2013. Name variants (Inc, Corp, punctuation) are merged.

3510(k) clearances (0 in 12 months)
2recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
NBWSystem, Test, Blood Glucose, Over The Counter3
PTCUric Acid Test System For At Home Prescription Use2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 15, 2013K122181EBCHEK BLOOD GLUCOSE MONITORING SYSTEM
Visgeneer, Inc., TW
NBW
Jan 19, 2010K091765EBCARRYON BLOOD GLUCOSE MONITORING SYSTEM
Visgeneer, Inc., TW
NBW
Dec 27, 2006K062555EBSENSOR BLOOD GLUCOSE MONITORING SYSTEM, MODEL EB-G
Visgeneer, Inc., TW
NBW

Latest recalls

DateFirm and productCodeLinked 510(k)
Sep 2, 2025Visgeneer, Inc.
Blood Uric Acid Monitoring System Each kit contains 1 meter, 1 lancing device, user manual, 10 lancets, and 10 test strips (10-count bottle)
Open, Classified		 PTCNone listed
Sep 2, 2025Visgeneer, Inc.
Blood Uric Acid Monitoring System Each kit contains 1 meter, 1 lancing device, user manual, 10 lancets, and 10 test strips (10-count bottle)
Open, Classified		 PTCNone listed
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