Orthophor, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthophor, LLC - FDA 510(k) Cleared Devices
Recent clearances: SURGIPHOR Wound Irrigation System
1
Total
1
Cleared
0
Denied
Orthophor, LLC has 1 FDA 510(k) cleared medical devices. Based in Philadelphia, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Orthophor, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Secure BioMed Evaluations as regulatory consultant.
FDA 510(k) Regulatory Record - Orthophor, LLC
1 devices