Wrightmedicaltechnologyinc is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wrightmedicaltechnologyinc - FDA 510(k) Cleared Devices
Recent clearances: Prophecy Preoperative Navigation Alignment System, PRO-DENSE LoVisc Bone Graft Substitute, Sterile PHALINX Hammertoe System
302
Total
291
Cleared
0
Denied
Wrightmedicaltechnologyinc has 291 FDA 510(k) cleared orthopedic devices. Based in Arlington, US.
Last cleared in 2023. Active since 1993.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Wrightmedicaltechnologyinc
302 devices
Cleared
Jan 27, 2023
Prophecy Preoperative Navigation Alignment System
Orthopedic
129d
Cleared
Jan 05, 2022
PRO-DENSE LoVisc Bone Graft Substitute
Orthopedic
90d
Cleared
Nov 16, 2021
Sterile PHALINX Hammertoe System
Orthopedic
57d
Cleared
Mar 10, 2021
PROPHECY Preoperative Navigation Alignment System
Orthopedic
167d
Cleared
Jan 08, 2021
ORTHOLOC 2 with 3Di Technology Pilon Fracture Plating System
Orthopedic
242d
Cleared
Oct 21, 2020
PRO-DENSE LoVisc Bone Graft Substitute
Orthopedic
233d
Cleared
Jun 08, 2020
The INBONE™ Total Ankle System, the INFINITY™ Total Ankle System and the...
Orthopedic
217d
Cleared
Aug 22, 2019
INFINITY Total Ankle System, INBONE Total Ankle System
Orthopedic
90d
Cleared
Aug 13, 2019
PROSTEP™ TBI™ (Tailors Bunion Implant) System
Orthopedic
123d
Cleared
Jun 06, 2019
PROSTEP TBC Implant System
Orthopedic
162d
Cleared
May 28, 2019
IGNITE Bone Void Filler
Orthopedic
90d
Cleared
May 14, 2019
ORTHOLOC™ 2 Lapidus with Rotation System
Orthopedic
60d
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