Medical Device Manufacturer · US , Bethel , CT

Kinetic Instruments, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2001

Recent clearances: TRANSCURE, MODEL 2910, SUNLITELED MODEL #2810

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Oct 18, 2002

TRANSCURE, MODEL 2910

Cleared Oct 02, 2001

SUNLITELED MODEL #2810