Medicon Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medicon Instruments, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Medicon Instruments, Inc. has 6 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 6 cleared submissions from 1994 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medicon Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medicon Instruments, Inc.
6 devices
Cleared
Jul 21, 1994
MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODES
General & Plastic Surgery
203d
Cleared
Jul 21, 1994
MEDICON INSTRUMENTS UNIPOLAR COAGULATION ELECTRODES
General & Plastic Surgery
203d
Cleared
Jul 01, 1994
DISSECTORS, FORCEPS, SCISSORS, DILATION SETS, AND GALL STONE COLLECTORS
General & Plastic Surgery
183d
Cleared
May 19, 1994
MEDICON INSTRUMENTS TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES
Cardiovascular
140d
Cleared
May 16, 1994
MEDICON INSTRUMENTS CHOLANGIOGRAPHY NEEDLES, GUIDE TUBES, INJECTION NEEDLES,...
General & Plastic Surgery
137d
Cleared
May 12, 1994
RETRACTORS, SPECULUM, CLIP APPLIER FOR TITANIUM CLIPS, 2-WAY STOP COCK,...
General & Plastic Surgery
133d