Home › Neotech Products LLC › NeoGlo Disposable
NeoGlo Disposable
Neotech Products LLC · Model 10812594013000 · UDI-DI 10812594013000
3
510(k) clearances
24
Adverse events
1
Recalls
28
Facilities
Description
3 Foot Cord Red Lights (Qty. 10)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-04-28 | Venoscope LLC | Excessive heating due to incorrect wire assembly process. |
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 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.