Blue Belt Technologies, Inc. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Blue Belt Technologies, Inc. has 21 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Latest FDA clearance: Dec 2025. Active since 2012. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Blue Belt Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Blue Belt Technologies, Inc.
10 devices
Cleared
Dec 05, 2025
REAL INTELLIGENCE™ CORI™ XT (CORI XT)
Orthopedic
88d
Cleared
Jun 25, 2025
CORIOGRAPH Pre-Op Planning and Modeling Services
Orthopedic
90d
Cleared
Nov 15, 2024
CORIOGRAPH Pre-Op Planning and Modeling Services
Orthopedic
106d
Cleared
Mar 18, 2024
Real Intelligence™ CORI™
Orthopedic
60d
Cleared
Aug 01, 2023
REAL INTELLIGENCE™ CORI™
Orthopedic
29d
Cleared
Aug 19, 2022
REAL INTELLIGENCE CORI
Orthopedic
113d
Cleared
Jul 27, 2022
Real Intelligence Cori
Orthopedic
117d
Cleared
Mar 29, 2022
REAL INTELLIGENCE CORI
Orthopedic
57d
Cleared
Mar 11, 2022
RI.HIP MODELER
Radiology
254d
Cleared
Nov 03, 2021
REAL INTELLIGENCE CORI (CORI)
Orthopedic
83d