Phalanx Innovations is one of 18477 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Phalanx Innovations - FDA 510(k) Cleared Devices
Recent clearances: OsteoBullet Compression Screw, StarFuse Interphalangeal Pin
2
Total
2
Cleared
0
Denied
Phalanx Innovations has 2 FDA 510(k) cleared medical devices. Based in Marietta, US.
Historical record: 2 cleared submissions from 2016 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Phalanx Innovations Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Wagoner Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Phalanx Innovations
2 devices