Home › RIVERPOINT MEDICAL, LLC › MaxLite Elite
MaxLite Elite
RIVERPOINT MEDICAL, LLC · Model MG6-HK-MX · UDI-DI 00840277406972
0
510(k) clearances
12
Adverse events
1
Recalls
71
Facilities
Description
MaxLite Elite G6 Hospital Kit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-06-11 | Integra LifeSciences Corp. | LED battery chargers may prematurely fail and will not charge the LED battery as intended |
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.
