Osteomed is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osteomed - FDA 510(k) Cleared Devices
Recent clearances: ExtremiLOCK Lateral Ankle Fusion Plates
12
Total
12
Cleared
0
Denied
Osteomed has 12 FDA 510(k) cleared medical devices. Based in Addison, US.
Last cleared in 2021. Active since 2012. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Osteomed Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Osteomed
12 devices
Cleared
Feb 24, 2021
ExtremiLOCK Lateral Ankle Fusion Plates
Orthopedic
89d
Cleared
May 19, 2017
OsteoMed PINNACLE Driver
Neurology
249d
Cleared
Apr 04, 2017
OsteoMed PINNACLE Driver
Dental
204d
Cleared
May 19, 2016
OsteoMed ExtremiLOCK Wrist Plating System
Orthopedic
36d
Cleared
Dec 21, 2015
OsteoMed ExtremiLOCK Wrist Plating System
Orthopedic
140d
Cleared
Sep 21, 2015
OsteoMed IMF Screw
Dental
140d
Cleared
Dec 18, 2014
OSTEOMED LOW PROFILE ORBITAL FLOOR PLATE SYSTEM
Dental
246d
Cleared
Feb 28, 2014
OSTEOMED EXTREMIFUSE SYSTEM
Orthopedic
24d
Cleared
Dec 06, 2013
OSTEOMED NEURO RONGEUR
Neurology
168d
Cleared
Dec 02, 2013
1ST MTP PLATE
Orthopedic
25d
Cleared
May 31, 2013
OSTEOMED EXTREMIFUSE SYSTEM
Orthopedic
101d
Cleared
Aug 22, 2012
OSTEOMED CRANIAL DISTRACTION SYSTEM
Neurology
113d