Medical Device Manufacturer · US , Mchenry , IL

Dentronix, Inc.

9 submissions · 9 cleared · Since 1977

9

Total

9

Cleared

0

Denied

Dentronix, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1977 to 1991. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Dentronix, Inc. Filter by specialty or product code using the sidebar.

9 devices

1–9 of 9

DENTRONIX MODEL 2000

K910202 · KMH Sterilizer, Dry Heat · General Hospital

DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEM

K880322 · KMH Sterilizer, Dry Heat · General Hospital

NEW PODIATRY PRODUCTS

K771005 · HTZ Instrument, Cutting, Orthopedic · General & Plastic Surgery

MODIFIED PODIATRY PRODUCTS

K771006 · HTZ Instrument, Cutting, Orthopedic · General & Plastic Surgery

CUTTER, P606 BONE

K770302 · FZT Cutter, Surgical · General & Plastic Surgery

NIPPER, NAIL, P610 ENGLISH

K770303 · FZT Cutter, Surgical · General & Plastic Surgery

CUTTER, P605 GENERAL PURPOSE

K770304 · FZT Cutter, Surgical · General & Plastic Surgery

CUTTER, P607 BONE

K770305 · FZT Cutter, Surgical · General & Plastic Surgery

NIPPER, PSO4 TISSUE

K770301 · FZT Cutter, Surgical · General & Plastic Surgery

Data Source

FDA 510(k) public files . 174,402 total devices indexed.