Rhausler, Inc. is one of 18477 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rhausler, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RT2 Trabeculite Titanium Cervical Cage System, RHAUSLER PLAGE ANTERIOR CERVICAL FUSION SYSTEM
2
Total
2
Cleared
0
Denied
Rhausler, Inc. has 2 FDA 510(k) cleared medical devices. Based in Arvada, US.
Historical record: 2 cleared submissions from 2011 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Rhausler, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Dionicia Reblando as regulatory consultant.
FDA 510(k) Regulatory Record - Rhausler, Inc.
2 devices