Implex Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Implex Corp. - FDA 510(k) Cleared Devices
Recent clearances: TRABECULAR METAL VERTEBRAL BODY REPLACEMENT, TRABECULAR METAL VERTEBRAL BODY REPLACEMENT, MODEL 06-165-011X1 AND 06-166-051X1, TRABECULAR METAL KNEE SYSTEM AUGMENTS
65
Total
61
Cleared
0
Denied
Implex Corp. has 61 FDA 510(k) cleared orthopedic devices. Based in Allendale, US.
Historical record: 61 cleared submissions from 1993 to 2005.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Implex Corp.
65 devices
Cleared
Sep 23, 2005
TRABECULAR METAL VERTEBRAL BODY REPLACEMENT
Orthopedic
64d
Cleared
Jun 17, 2005
TRABECULAR METAL VERTEBRAL BODY REPLACEMENT, MODEL 06-165-011X1 AND 06-166-051X1
Orthopedic
38d
Cleared
Dec 21, 2004
TRABECULAR METAL KNEE SYSTEM AUGMENTS
Orthopedic
300d
Cleared
Sep 30, 2004
TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZ
Orthopedic
204d
Cleared
Jul 14, 2004
THE TRABECULAR METAL RECONSTRUCTION SYSTEM, MODEL 10-340-XXXXX
General & Plastic Surgery
112d
Cleared
Jan 08, 2004
NEXGEN TRABECULAR METAL TIBIAL CONE AUGMENTS
Orthopedic
197d
Cleared
Nov 19, 2003
THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM, MODEL 06-165-ZZZZ
Orthopedic
27d
Cleared
Oct 31, 2003
HEDROCEL VERTEBRAL BODY REPLACEMENT
Orthopedic
77d
Cleared
Oct 02, 2003
THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM MODEL 10-330
General & Plastic Surgery
64d
Cleared
Sep 23, 2003
MODIFICATION TO THE TRABECULAR METAL GLENOID - BIGLIANI/FLATOW THE COMPLETE...
Orthopedic
139d
Cleared
Aug 21, 2003
MODIFICATION TO HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM
General & Plastic Surgery
28d
Cleared
Aug 06, 2003
THE NEXGEN KNEE SYSTEM UNCEMENTED COMPONENTS
Orthopedic
90d
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