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RightLance
VISGENEER, INC. · Model RC-AD-VIU · UDI-DI 04712558762694
10
510(k) clearances
250
Adverse events
1
Recalls
87
Facilities
Description
reusable lancing device that is to be cleaned and disinfected between each use, to be used with the sterile single-use lancets
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-07-25 | Home Health US, Incorporated | Due to incorrect/lack of Unique Device Identifier (UDI) codes. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.