Medical Device Manufacturer · US , Spring Valley , CA

Lumalite, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1999

Recent clearances: VERACAM, LUMALITE CURE LIGHT, MODEL 2100, LUMA LIGHT 2000 CURE LIGHT

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Lumalite, Inc. Dental ✕

3 devices

1-3 of 3

Cleared Aug 30, 2002

Cleared Oct 19, 2000

LUMALITE CURE LIGHT, MODEL 2100

Cleared Aug 31, 1999

LUMA LIGHT 2000 CURE LIGHT