Electro-Biology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Electro-Biology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EBI OMEGA 21 SYSTEM, EBI XFIX DYNAFIX SYSTEM HA COATED SCREWS, EBI XFIX DFS RAIL SYSTEM
28
Total
22
Cleared
0
Denied
Electro-Biology, Inc. has 22 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 22 cleared submissions from 1983 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 - Electro-Biology, Inc.
28 devices
Cleared
Oct 08, 1999
EBI OMEGA 21 SYSTEM
Orthopedic
87d
Cleared
Sep 23, 1999
EBI XFIX DYNAFIX SYSTEM HA COATED SCREWS
Orthopedic
70d
Cleared
Aug 19, 1999
EBI XFIX DFS RAIL SYSTEM
Orthopedic
71d
Cleared
Apr 29, 1999
EBI OMEGA 21 SYSTEM
Orthopedic
87d
Cleared
Apr 29, 1999
EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEM
Orthopedic
28d
Cleared
Apr 23, 1999
EBI VUECATH ENDOSCOPIC SYSTEN
Orthopedic
70d
Cleared
Apr 14, 1999
MODIFICATION OF: EBI SPINELINK SYSTEM
Orthopedic
20d
Cleared
Jan 19, 1999
EBI SPINELINK SYSTEM
Orthopedic
68d
Cleared
Oct 08, 1998
EBI VUECATH ENDOSCOPIC SPINAL SYSTEM
Orthopedic
83d
Cleared
Aug 28, 1998
MODIFICATION TO EBI SPINELINK SYSTEM
Orthopedic
10d
Cleared
Jul 08, 1998
EBI DFS JOINT FIXATOR, MODEL 02800
Orthopedic
75d
Cleared
Aug 20, 1997
EBI SPINELINK SYSTEM
Orthopedic
83d