Trilliant Surgical, Ltd. is one of 18450 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trilliant Surgical, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Minimally Invasive Bunion Plating System, Sniper Staple System, Gridlock Ankle Plating System
14
Total
14
Cleared
0
Denied
Trilliant Surgical, Ltd. has 14 FDA 510(k) cleared orthopedic devices. Based in Round Rock, US.
Historical record: 14 cleared submissions from 2007 to 2017.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by The Orthomedix Group and The OrthoMedix Group, Inc..
FDA 510(k) Regulatory Record - Trilliant Surgical, Ltd.
14 devices
Cleared
Nov 16, 2017
Minimally Invasive Bunion Plating System
Orthopedic
120d
Cleared
Apr 20, 2017
Sniper Staple System
Orthopedic
240d
Cleared
Apr 22, 2016
Gridlock Ankle Plating System
Orthopedic
86d
Cleared
Jan 14, 2016
Tiger Cannulated Screw System
Orthopedic
56d
Cleared
May 08, 2013
GRIDLOCK PLATING SYSTEM
Orthopedic
30d
Cleared
Feb 15, 2013
GRIDLOCK PLATING SYSTEM
Orthopedic
92d
Cleared
Nov 07, 2012
HAMMER TOE IMPLANT
Orthopedic
43d
Cleared
Aug 20, 2012
GRIDLOCK PLATING SYSTEM
Orthopedic
96d
Cleared
Jun 04, 2012
TRILLIANT SURGICAL K-WIRES
Orthopedic
62d
Cleared
Dec 06, 2011
DISCO SUBTALAR IMPLANT
Orthopedic
160d
Cleared
Oct 20, 2011
TIGER HEADLESS CANNULATED SCREWS
Orthopedic
30d
Cleared
Feb 08, 2011
TRILLIANT SURGICAL SUBTALAR IMPLANT
Orthopedic
103d