FDA Device Intelligence
Home › ABOUND Diagnostics, Inc. › VivaGuard Lancets (28G)

VivaGuard Lancets (28G)

ABOUND Diagnostics, Inc. · Model VGL01-2U2 · UDI-DI 00840423500103

QRLQRKFMK
10
510(k) clearances
250
Adverse events
1
Recalls
87
Facilities

Description

VivaGuard Lancets (28G)

Recalls

DateFirmReason
2025-07-25Home Health US, IncorporatedDue to incorrect/lack of Unique Device Identifier (UDI) codes.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data 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.