Orthocon, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthocon, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Permatage XT Settable Bone Putty, Permatage Flowable, Settable Hemostatic Bone Paste, Montage Flowable Settable, Resorbable Bone Paste (Burr Hole Cover)
36
Total
36
Cleared
0
Denied
Orthocon, Inc. has 36 FDA 510(k) cleared medical devices. Based in Stamford, US.
Latest FDA clearance: Jun 2026. Active since 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Orthocon, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mcra, LLC and Abyrx, Inc..
FDA 510(k) Regulatory Record - Orthocon, Inc.
36 devices
Cleared
Jun 15, 2026
Permatage XT Settable Bone Putty
Neurology
60d
Cleared
Jun 03, 2026
Permatage Flowable, Settable Hemostatic Bone Paste
Orthopedic
34d
Cleared
Mar 16, 2026
Montage Flowable Settable, Resorbable Bone Paste (Burr Hole Cover)
Neurology
165d
Cleared
Mar 13, 2026
Permatage Flowable, Settable Bone Paste
Neurology
109d
Cleared
Jan 02, 2026
MONTAGE XT Cranial Cement
Neurology
30d
Cleared
Dec 05, 2024
MONTAGE Settable, Resorbable Bone Putty MONTAGE-QS Settable, Resorbable Bone...
Orthopedic
21d
Cleared
Nov 18, 2024
Montage-XT Settable Bone Putty
Orthopedic
6d
Cleared
Sep 26, 2024
Permatage Settable Bone Putty
Neurology
164d
Cleared
Aug 21, 2024
Montage-XT Settable, Resorbable Bone Putty
Orthopedic
289d
Cleared
Jul 29, 2024
Montage Settable Bone Putty
Orthopedic
17d
Cleared
Feb 16, 2024
Montage Flowable Settable, Resorbable Bone Paste
Neurology
158d
Cleared
Oct 12, 2023
MONTAGE-QS Settable, Resorbable Bone Putty
Neurology
143d