Medical Device Manufacturer · US , Mchenry , IL

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

9 submissions · 9 cleared · Since 1977

Total

Cleared

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.

Dentronix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

9 devices

1-9 of 9

Cleared Mar 13, 1991

DENTRONIX MODEL 2000

K910202 · KMH

General Hospital · 62d

Cleared Jul 13, 1988

DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEM

K880322 · KMH

General Hospital · 168d

Cleared Jun 17, 1977

NEW PODIATRY PRODUCTS

K771005 · HTZ

General & Plastic Surgery · 15d

Cleared Jun 17, 1977

MODIFIED PODIATRY PRODUCTS

K771006 · HTZ

General & Plastic Surgery · 15d

Cleared Mar 09, 1977

CUTTER, P606 BONE

K770302 · FZT

General & Plastic Surgery · 21d

Cleared Mar 09, 1977

NIPPER, NAIL, P610 ENGLISH

K770303 · FZT

General & Plastic Surgery · 21d

Cleared Mar 09, 1977

CUTTER, P605 GENERAL PURPOSE

K770304 · FZT

General & Plastic Surgery · 21d

Cleared Mar 09, 1977

CUTTER, P607 BONE

K770305 · FZT

General & Plastic Surgery · 21d

Cleared Mar 07, 1977

NIPPER, PSO4 TISSUE

K770301 · FZT

General & Plastic Surgery · 19d

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

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

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