Visgeneer, Inc.
Visgeneer, Inc. holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2013, with 2 FDA device recalls on record.
Top product codes for Visgeneer, Inc.
FDA recalls by Visgeneer, Inc.
- Z-2501-2025 — Blood Uric Acid Monitoring System Each kit contains 1 meter, 1 lancing device, user manual, 10 lancets, and 10 test strips (10-count bottle)
- Z-2500-2025 — Blood Uric Acid Monitoring System Each kit contains 1 meter, 1 lancing device, user manual, 10 lancets, and 10 test strips (10-count bottle)
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Visgeneer, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.