Providence Medical Technology, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Providence Medical Technology, Inc. has 19 FDA 510(k) cleared orthopedic devices. Based in Lafayette, US.
Latest FDA clearance: Nov 2025. 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 Technologies and R. Dubois Consulting. 1 device has linked clinical trial registered on ClinicalTrials.gov.
19 devices
Cleared
Nov 20, 2025
CORUS-LX Implant
Orthopedic
55d
Cleared
Jul 30, 2025
CORUS™ Navigation System-GX
Orthopedic
117d
Cleared
Jul 10, 2025
CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant
Orthopedic
20d
Cleared
CT
Jun 25, 2024
PMT Posterior Cervical Stabilization System (PCSS)
Orthopedic
70d
Cleared
May 03, 2024
CORUS Navigation Access System
Orthopedic
58d
Cleared
Dec 19, 2023
PMT Facet Fixation System, Lumbar (PMT FFS-LX)
Orthopedic
267d
Cleared
Aug 11, 2023
PMT Expandable Cage (PMT EXP)
Orthopedic
190d
Cleared
Dec 09, 2022
PMT Facet Fixation System (PMT FFS)
Orthopedic
252d
Cleared
Oct 15, 2021
CORUS Spinal System-X
Orthopedic
57d
Cleared
Oct 11, 2019
PMT Facet Screw
Orthopedic
294d
Cleared
Mar 08, 2019
CORUS Spinal System
General & Plastic Surgery
32d
Cleared
May 18, 2018
DTRAX Spinal System
Orthopedic
45d