Gexfix International Corp. is one of 20126 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gexfix International Corp. - FDA 510(k) Cleared Devices
Recent clearances: Gexfix External Fixation
1
Total
1
Cleared
0
Denied
Gexfix International Corp. has 1 FDA 510(k) cleared medical devices. Based in Boca Raton, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Gexfix International Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Donawa Lifescience Consulting Srl as regulatory consultant.
FDA 510(k) Regulatory Record - Gexfix International Corp.
1 devices