Osteoready, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osteoready, LLC - FDA 510(k) Cleared Devices
Recent clearances: OsteoReady Dental Implant System
2
Total
2
Cleared
0
Denied
Osteoready, LLC has 2 FDA 510(k) cleared medical devices. Based in Seattle, US.
Historical record: 2 cleared submissions from 2015 to 2018. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Osteoready, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sterling Medical Registration as regulatory consultant.
FDA 510(k) Regulatory Record - Osteoready, LLC
2 devices