Dentsleeve Pty., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dentsleeve Pty., Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Dentsleeve Pty., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Golden, US.
Historical record: 3 cleared submissions from 1998 to 2001. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Dentsleeve Pty., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dentsleeve Pty., Ltd.
3 devices
Cleared
Oct 19, 2001
MARK II/MARK III MANOMETRIC PERFUSION PUMP
Gastroenterology & Urology
29d
Cleared
May 17, 1999
MANOMETRIC ASSEMBLIES
Gastroenterology & Urology
210d
Cleared
Jun 08, 1998
MARK II CO2 FLUSH MANOMETRIC PERFUSION PUMP & MARK II MANOMETRIC PERFUSION PUMP
Gastroenterology & Urology
87d