Tfx Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tfx Medical, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Tfx Medical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Jeffrey, US.
Historical record: 4 cleared submissions from 2000 to 2002. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Tfx Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tfx Medical, Inc.
4 devices
Cleared
Jun 26, 2002
MODIFIED TFX MEDICAL SAFETY NEEDLE WITH INTRODUCER
Gastroenterology & Urology
89d
Cleared
Jun 25, 2002
MODIFIED TFX MEDICAL SAFETY NEEDLE WITH INTRODUCER
Gastroenterology & Urology
90d
Cleared
May 02, 2000
TFX MEDICAL SAFETY NEEDLE WITH INTRODUCER
General Hospital
64d
Cleared
Mar 24, 2000
TFX MEDICAL INTRODUCER ASSEMBLY
Cardiovascular
183d