Medical Device Manufacturer · US , Lafayette , CA

Providence Medical Technology, Inc. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 2012

Recent clearances: CORUS™ Navigation System-GN, CORUS™ Posterior Cervical Stabilization System 3D (CORUS™ PCSS 3D), CORUS-LX Implant

21
Total
21
Cleared
0
Denied

Providence Medical Technology, Inc. has 21 FDA 510(k) cleared orthopedic devices. Based in Lafayette, US.

Latest FDA clearance: Jun 2026. Active since 2012.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by R. Dubois Consulting, LLC, Empirical Testing Corporation and Empirical Technologies. 1 device has linked clinical trial registered on ClinicalTrials.gov.

FDA 510(k) Regulatory Record - Providence Medical Technology, Inc.

21 devices
1-12 of 21
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