Medical Device Manufacturer · US , Mchenry , IL

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

9 submissions · 9 cleared · Since 1977

9

Total

9

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dentronix, Inc. General Hospital ✕

2 devices

1-2 of 2

Cleared Mar 13, 1991

DENTRONIX MODEL 2000

General Hospital · 62d

Cleared Jul 13, 1988

DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEM

General Hospital · 168d