Ximed/Prosure/Injectx is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ximed/Prosure/Injectx - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Ximed/Prosure/Injectx has 9 FDA 510(k) cleared medical devices. Based in San Jose, US.
Historical record: 9 cleared submissions from 1995 to 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ximed/Prosure/Injectx Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ximed/Prosure/Injectx
9 devices
Cleared
Jan 04, 2001
ELECTROSURGICAL PROBES AND DEVICES-GELTX
General & Plastic Surgery
162d
Cleared
Mar 01, 2000
PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES
General & Plastic Surgery
83d
Cleared
Dec 11, 1998
INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEX
General & Plastic Surgery
88d
Cleared
Dec 11, 1998
INJECTION NEEDLE PROBE/DEVICE-TUNIS
Gastroenterology & Urology
46d
Cleared
May 12, 1998
ISOLATED SALINE ELECTRODES/PROBES/DEVICES-SALINETRODE
Gastroenterology & Urology
40d
Cleared
Feb 10, 1998
ISOLATED ELECTROSURGICAL PROBES AND DEVICES-SALINETRODE
General & Plastic Surgery
76d
Cleared
Jan 07, 1998
ELECTRODES/PROBES/DEVICES
Gastroenterology & Urology
26d
Cleared
Nov 12, 1996
ELECTROSURGICAL PROBES & DEVICES
General & Plastic Surgery
133d
Cleared
Jan 31, 1995
BIPOLAR ELECTROSURGICAL PROBES AND INSTRUMENTS
General & Plastic Surgery
117d