Karl Storz Endoscopy is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Karl Storz Endoscopy - FDA 510(k) Cleared Devices
Recent clearances: FISCH TITANIUM MIDDLE EAR PROSTHESES, PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIX, KSEA POWERSHAVER SYSTEM S2
35
Total
35
Cleared
0
Denied
Karl Storz Endoscopy has 35 FDA 510(k) cleared medical devices. Based in Culver City, US.
Historical record: 35 cleared submissions from 1995 to 2005.
Browse the FDA 510(k) cleared devices submitted by Karl Storz Endoscopy Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by KARL STORZ Endoscopy-America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Karl Storz Endoscopy
35 devices
Cleared
Jan 24, 2005
FISCH TITANIUM MIDDLE EAR PROSTHESES
Ear, Nose, Throat
47d
Cleared
Jun 02, 2003
PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
Orthopedic
77d
Cleared
Apr 02, 2003
KSEA POWERSHAVER SYSTEM S2
Orthopedic
90d
Cleared
Feb 21, 2003
AUTOCON II 200 ELECTROSURGICAL GENERATOR
General & Plastic Surgery
88d
Cleared
Dec 02, 2002
KSEA SPINOSCOPE
Orthopedic
69d
Cleared
Aug 16, 2002
MODULITH SLK LITHOTRIPTER
Gastroenterology & Urology
441d
Cleared
Aug 15, 2002
KSEA QUADRO SWITCH
Gastroenterology & Urology
78d
Cleared
Feb 26, 2002
BIOABSORBABLE INTERFERENCE SCREW MEGAFIX
Orthopedic
162d
Cleared
Sep 10, 2001
KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR
General & Plastic Surgery
90d
Cleared
Apr 09, 2001
KSEA UNIVERSAL LAPAROMAT LAPAROSCOPIC SUCTION AND IRRIGATION PUMP
General & Plastic Surgery
42d
Cleared
Feb 02, 2001
X-RAY SYSTEM XR-MX
Radiology
36d
Cleared
Jul 19, 2000
KSEA BIPOLAR COAGULATING ELECTRODES
Neurology
54d