Tecnadyne Scientific, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tecnadyne Scientific, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Tecnadyne Scientific, Inc. has 5 FDA 510(k) cleared medical devices. Based in Vero Beach, US.
Historical record: 5 cleared submissions from 1990 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Tecnadyne Scientific, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tecnadyne Scientific, Inc.
5 devices
Cleared
Apr 29, 1994
TECNADYNE 20/20 FOG INHIBITOR KIT
General & Plastic Surgery
88d
Cleared
Apr 26, 1994
TECNADYNE ENDOSCOPIC INSTRUMENT HOLDER
General & Plastic Surgery
60d
Cleared
Aug 02, 1991
TECNADYNE SURGI-SQUEEZE INFUSION PUMP
General Hospital
150d
Cleared
Jul 22, 1991
BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFF
Cardiovascular
77d
Cleared
Oct 26, 1990
BAXTER SINGLE PATIENT USE PRESSURE INFUSOR
General Hospital
24d