Medical Device Manufacturer · US , Chatham , NJ

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

8 submissions · 8 cleared · Since 1999

8

Total

8

Cleared

0

Denied

Immedica, Inc. has 8 FDA 510(k) cleared medical devices. Based in Chatham, US.

Historical record: 8 cleared submissions from 1999 to 2003. Primary specialty: Orthopedic.

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

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

8 devices

1-8 of 8

Cleared Jan 22, 2003

CONCERT CRANIOPLAST

Neurology · 90d

Cleared Feb 08, 2002

CONCERT RADIOPAQUE BONE CEMENT

Orthopedic · 87d

Cleared Dec 15, 2000

TRANSFX ANGLED RODS

Orthopedic · 63d

Cleared Jul 07, 2000

EXTERNAL FIXATION ANCHOR PIN

Orthopedic · 81d

Cleared Jun 15, 2000

TRANS FX ADJUSTABLE PIN TO BAR CLAMP

Orthopedic · 72d

Cleared Jul 22, 1999

TRANSFX MULTI PIN CLAMP

Orthopedic · 63d

Cleared May 17, 1999

TRANSFX INTERMEDIATE EXTERNAL FIXATION SYSTEM,TRANSFX SMALL EXTERNAL FIXATION...

Orthopedic · 63d

Cleared Mar 04, 1999

TRANSFX EXTERNAL FIXATION SYSTEM

Orthopedic · 87d