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VF1000LED Vein locator
FABINJECT LLC · Model VF1000LEDBX1 · UDI-DI 00850064466348
3
510(k) clearances
24
Adverse events
1
Recalls
28
Facilities
Description
A device designed to locate veins through cutaneous transillumination.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-04-28 | Venoscope LLC | Excessive heating due to incorrect wire assembly process. |
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
