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