Carre Technologies, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Carre Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Hexoskin Medical System (7100-00016)
1
Total
1
Cleared
0
Denied
Carre Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Montreal, CA.
Latest FDA clearance: Nov 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Carre Technologies, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Carre Technologies, Inc.
1 devices