X-Nav Technologies, LLC is one of 17607 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
X-Nav Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: X-Guide Surgical Navigation System, X-Guide Surgical Navigation System, X-Guide® Surgical Navigation System
6
Total
6
Cleared
0
Denied
X-Nav Technologies, LLC has 6 FDA 510(k) cleared medical devices. Based in Lansdale, US.
Latest FDA clearance: Aug 2026. Active since 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by X-Nav Technologies, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - X-Nav Technologies, LLC
6 devices
Cleared
Aug 28, 2026
X-Guide Surgical Navigation System
Dental
261d
Cleared
Feb 21, 2024
X-Guide Surgical Navigation System
Dental
217d
Cleared
Feb 01, 2022
X-Guide® Surgical Navigation System
Dental
243d
Cleared
May 21, 2020
X-Guide® Surgical Navigation System
Dental
69d
Cleared
Feb 03, 2020
X-Guide Surgical Navigation System
Dental
137d
Cleared
Oct 08, 2015
X-Guide Surgical Navigation System
Dental
251d