Blue Belt Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Blue Belt Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: REAL INTELLIGENCE™ CORI™, REAL INTELLIGENCE™ CORI™ XT (CORI XT), CORIOGRAPH Pre-Op Planning and Modeling Services
22
Total
22
Cleared
0
Denied
Blue Belt Technologies, Inc. has 22 FDA 510(k) cleared orthopedic devices. Based in Pittsburgh, US.
Latest FDA clearance: Mar 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.
FDA 510(k) Regulatory Record - Blue Belt Technologies, Inc.
22 devices
Cleared
Mar 26, 2026
REAL INTELLIGENCE™ CORI™
Orthopedic
30d
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
Cleared
Jun 12, 2020
REAL INTELLIGENCE CORI (CORI)
Orthopedic
53d