Biodynamic Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biodynamic Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ULTIMAX TROCHANTERIC INTRAMEDULLARY ROD SYSTEM, ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEM, ULTIMAX CORTICAL BONE SCREWS
30
Total
28
Cleared
0
Denied
Biodynamic Technologies, Inc. has 28 FDA 510(k) cleared orthopedic devices. Based in Arlington, US.
Historical record: 28 cleared submissions from 1985 to 1999.
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 - Biodynamic Technologies, Inc.
30 devices
Cleared
Mar 31, 1999
ULTIMAX TROCHANTERIC INTRAMEDULLARY ROD SYSTEM
Orthopedic
48d
Cleared
Mar 17, 1999
ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEM
Orthopedic
29d
Cleared
Mar 17, 1999
ULTIMAX CORTICAL BONE SCREWS
Orthopedic
27d
Cleared
Jun 01, 1998
ULTIMAX DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM
Orthopedic
59d
Cleared
Apr 03, 1998
BTI HUMERAL INTRAMEDULLARY ROD SYSTEM
Orthopedic
81d
Cleared
Mar 12, 1998
BTI LARGE (7.0MM) CANNULATED TRANSFIXING SCREWS
Orthopedic
83d
Cleared
Aug 29, 1997
BTI CORTICAL BONE SCREWS
Orthopedic
64d
Cleared
Apr 21, 1997
BTI DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM
Orthopedic
41d
Cleared
Nov 13, 1996
EZ-FIX CANNULATED SCREW SYSTEM
Orthopedic
124d
Cleared
Nov 04, 1996
EZ-FIX SMALL CANNULATED SCREW SYSTEM
Orthopedic
95d
Cleared
Oct 23, 1996
EZ-FIX COMPRESSION HIP/SUPRACONDYLAR SCREW (CHS) SYSTEM
Orthopedic
93d
Cleared
Sep 25, 1996
EZ-6 PROXIMAL HUMERAL INTERAMEDULLARY ROD SYSTEM
Orthopedic
86d