Ebi, L.P. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ebi, L.P. - FDA 510(k) Cleared Devices
Recent clearances: POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTURE ANTERIOR FIXATION SYSTEM, POLARIS SPINAL SYSTEM, PEANUT GROWTH CONTROL PLATING SYSTEM
95
Total
94
Cleared
0
Denied
Ebi, L.P. has 94 FDA 510(k) cleared orthopedic devices. Based in Parsippany, US.
Historical record: 94 cleared submissions from 1997 to 2010.
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 - Ebi, L.P.
95 devices
Cleared
Jun 23, 2010
POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTURE ANTERIOR FIXATION SYSTEM
Orthopedic
126d
Cleared
May 17, 2010
POLARIS SPINAL SYSTEM
Orthopedic
111d
Cleared
Apr 16, 2010
PEANUT GROWTH CONTROL PLATING SYSTEM
Orthopedic
119d
Cleared
Feb 04, 2010
ESL SPINAL SYSTEM
Orthopedic
167d
Cleared
Dec 01, 2009
BIOMET VISION FOOTRING SYSTEM
Orthopedic
62d
Cleared
Oct 15, 2009
C-THRU SPINAL SYSTEM
Orthopedic
72d
Cleared
Aug 07, 2009
IBEX SPINAL SYSTEM
Orthopedic
88d
Cleared
Jul 30, 2009
5.5 HELICAL FLANGE SPINAL SYSTEM, POLARIS COMPONENTS
Orthopedic
184d
Cleared
Jul 01, 2009
POLARIS SPINAL SYSTEM
Orthopedic
125d
Cleared
Jan 14, 2009
EXPANDABLE PEEK-OPTIMA IMPLANT
Orthopedic
146d
Cleared
Nov 13, 2008
BIOMET ANTERIOR LUMBAR PLATE
Orthopedic
101d
Cleared
Apr 18, 2007
PRO OSTEON 500R
Orthopedic
166d
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