Medical Device Manufacturer · US , Mchenry , IL

Tri-Med, Inc. - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 1977

29

Total

29

Cleared

0

Denied

Tri-Med, Inc. has 29 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 29 cleared submissions from 1977 to 2004.

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

Tri-Med, 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 - Tri-Med, Inc.

29 devices

1-12 of 29

Cleared Mar 12, 2004

TRIMED BEARING PLATE

Orthopedic · 52d

Cleared Feb 05, 2004

TRIMED RADIAL BULLET

Orthopedic · 322d

Cleared Jun 06, 2001

Orthopedic · 103d

Cleared May 28, 1996

PARACENTESIS TRAYS

General & Plastic Surgery · 14d

Cleared Jan 28, 1988

HUDSON CRANINAL BURRS

Neurology · 37d

Cleared Apr 02, 1985

TRI-MED MODEL 112 MOISTURE TRAP

Anesthesiology · 36d

Cleared Apr 02, 1985

TRI-MED MODEL 126 SAMPLE LINE W/EXTENDED LIFE NAFI

Anesthesiology · 36d

Cleared Apr 02, 1985

TRI-MED MODEL 105 SPECIAL AIRWAY ADAPTOR

Anesthesiology · 36d

Cleared Dec 04, 1984

RESPIRATION & HEART RATE MONITOR 530

Anesthesiology · 77d

Cleared Nov 13, 1984

TRI-MED 610 CAPNOSTAT GAS ANALYZER

Anesthesiology · 84d

Cleared Oct 09, 1984

48 HOUR SET CHANGES

General Hospital · 112d

Cleared Apr 20, 1984

General Hospital · 92d