Leonhard Lang GmbH is one of 5103 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Leonhard Lang GmbH - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Leonhard Lang GmbH has 17 FDA 510(k) cleared cardiovascular devices. Based in Stillwater, US.
Historical record: 17 cleared submissions from 2002 to 2014.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
Leonhard Lang GmbH — FDA 510(k) Products and Clearance History
17 devices
Cleared
Dec 02, 2014
Skintact, various other tradenames
Cardiovascular
64d
Cleared
Jul 29, 2014
SKINTACT
General & Plastic Surgery
152d
Cleared
May 21, 2014
SKINTACT
Neurology
99d
Cleared
Feb 08, 2011
SKINTACT RADIOTRANSPARENT MULTIFUNCTION ELECTRODES
Cardiovascular
102d
Cleared
Aug 21, 2009
SKINTACT AND VARIOUS OTHER TRADENAMES
Cardiovascular
23d
Cleared
Sep 24, 2008
SKINTACT PEDIATRIC MULTIFUNCTION ELECTRODES WITH DH03 GEL
Cardiovascular
132d
Cleared
Feb 01, 2008
SKINTACT PRE-WIRED ECG ELECTRODES WITH CONDUCTIVE ADHESIVE
Cardiovascular
17d
Cleared
Nov 16, 2007
SKINTACT AND VARIOUS OTHER TRADENAMES
Cardiovascular
14d
Cleared
Oct 05, 2007
SKINTACT MULTIFUNCTIONAL ELECTRODES WITH DH02 GEL WITH DIFFERENT CONNECTORS...
Cardiovascular
56d
Cleared
Nov 21, 2006
SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATE WITH NH 04 GEL
General & Plastic Surgery
35d
Cleared
Sep 07, 2004
SKINTACT MULTIFUNCTION ELECTRODES, MODEL DF 21
Cardiovascular
57d
Cleared
Feb 24, 2004
SKINTACT ECG ELECTRODE
Cardiovascular
21d
Cleared
Apr 14, 2003
SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATES
General & Plastic Surgery
70d
Cleared
Mar 04, 2003
SKINTACT ECG TAB ELECTRODE
Cardiovascular
13d
Cleared
Jan 16, 2003
SKINTACT
Cardiovascular
52d
Cleared
Jan 16, 2003
SKINTACT ECG ELECTRODES WITH KL 02 LIQUID GEL
Cardiovascular
24d
Cleared
Nov 14, 2002
SKINTACT ECG ELECTRODE
Cardiovascular
27d