Core Dynamics, Inc. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Core Dynamics, Inc. has 23 FDA 510(k) cleared medical devices. Based in Jacksonville, US.
Historical record: 23 cleared submissions from 1990 to 1999. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Core Dynamics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Core Dynamics, Inc.
23 devices
Cleared
Sep 24, 1999
CORE AUDIBLE TROCAR II
General & Plastic Surgery
80d
Cleared
Sep 01, 1999
CORE POUCH
General & Plastic Surgery
64d
Cleared
Jan 22, 1996
LAPAROSCOPIC KNITTER
General & Plastic Surgery
80d
Cleared
Oct 20, 1995
LAPAROSCOPIC TROCAR OBTURATOR, 5MM, 10/11MM, 10/12MM
General & Plastic Surgery
92d
Cleared
Oct 16, 1995
LAPAROSCOPIC TROCAR
General & Plastic Surgery
88d
Cleared
May 05, 1995
CANNUAL AND TROCAR, SUPERPUBIC
Obstetrics & Gynecology
91d
Cleared
Jul 28, 1994
CORE DYNAMICS' LAPAROSCOPIC SMOKE ELIMINATOR
General & Plastic Surgery
38d
Cleared
May 18, 1994
LAPAROSCOPIC/SUCTION/IRRIGATION PROBE
General & Plastic Surgery
163d
Cleared
Mar 17, 1994
ENDOSCOPIC TRANSMURAL SUTURE NEEDLE SET
Obstetrics & Gynecology
318d
Cleared
Jan 11, 1994
ENTREE BLUNT TIP TROCAR AND ADAPTER
Obstetrics & Gynecology
263d
Cleared
Jan 11, 1994
ENTREE CANNULA FASCIA ANCHORS
Gastroenterology & Urology
263d
Cleared
Nov 12, 1993
BIFURCATED SUCTION/IRRIGAT TUBING SET W/PUSH BUTTO
General & Plastic Surgery
318d