Therex Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Therex Corp. - FDA 510(k) Cleared Devices
Recent clearances: LOW PROFILE TITANIUM MODEL CATALOG #1003, LOW PROFILE TITANIUM MODEL CATALOG #1003, THEREX LOW PROFILE TITANIUM MODEL 1.0MM I.D./1.8MM O.D.
26
Total
23
Cleared
0
Denied
Therex Corp. has 23 FDA 510(k) cleared general hospital devices. Based in Walpole, US.
Historical record: 23 cleared submissions from 1988 to 1995.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Therex Corp.
26 devices
Cleared
Sep 13, 1995
LOW PROFILE TITANIUM MODEL CATALOG #1003
General Hospital
72d
Cleared
Sep 08, 1995
LOW PROFILE TITANIUM MODEL CATALOG #1003
General Hospital
71d
Cleared
Jul 06, 1995
THEREX LOW PROFILE TITANIUM MODEL 1.0MM I.D./1.8MM O.D.
General Hospital
36d
Cleared
Apr 13, 1995
A2 DETACHED DUAL PORT SYSTEM
General Hospital
84d
Cleared
Mar 23, 1995
1.0MM 1.8MMO.D. POLYURETHANE DETACHED MODEL
General Hospital
69d
Cleared
Aug 19, 1994
THEREX LOW-PROFILE PORT - TITANIUM MODEL
General Hospital
91d
Cleared
Mar 22, 1994
THEREX LOW-PROFILE PORT
General Hospital
167d
Cleared
Mar 22, 1994
THEREX LOW-PROFILE PORT-TITANIUM
General Hospital
166d
Cleared
Mar 22, 1994
THEREX LOW PROFILE PORT-TITANIUM MODEL
General Hospital
96d
Cleared
Feb 23, 1994
THEREX LOW-PROFILE PORT DETACHED CATHETER SYSTEM
General Hospital
231d
Cleared
Feb 23, 1994
THEREX LOW-PROFILE PORT 1.5MM I.D. X 2.7MM O.D. DETACHED CATHETER SYSTEM
General Hospital
229d
Cleared
Feb 09, 1994
THEREX LOW-PROFILE PORT .6MM I.D 2.3MM O.D.
General Hospital
265d