Integra LifeSciences Corporation - FDA 510(k) Cleared Devices
65
Total
65
Cleared
0
Denied
Integra LifeSciences Corporation has 65 FDA 510(k) cleared medical devices. Based in Planisboro, US.
Latest FDA clearance: Oct 2025. Active since 2004. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Integra LifeSciences Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Integra LifeSciences Corporation
65 devices
Cleared
Oct 08, 2025
CUSA® Clarity Ultrasonic Surgical Aspirator System
General & Plastic Surgery
176d
Cleared
Apr 09, 2025
AURORA® Surgiscope® System (ASX15/60)
Neurology
28d
Cleared
Jul 11, 2024
CUSA® Clarity Ultrasonic Surgical Aspirator System
Obstetrics & Gynecology
142d
Cleared
Jul 11, 2023
CUSA Clarity Ultrasonic Surgical Aspirator System
General & Plastic Surgery
144d
Cleared
Aug 22, 2022
CUSA Clarity Ultrasonic Surgical Aspirator System
General & Plastic Surgery
60d
Cleared
Jul 15, 2022
CUSA Clarity Ultrasonic Surgical Aspirator System
General & Plastic Surgery
28d
Cleared
Oct 08, 2021
INTEGRA Wound Matrix (Macro-Channels)
General & Plastic Surgery
262d
Cleared
Jul 27, 2021
Integra DigiFuse Cannulated Intramedullary Fusion System,Integra Total Foot...
Orthopedic
204d
Cleared
Nov 20, 2020
Codman Surgical Patties & Strips
Neurology
353d
Cleared
Jun 29, 2020
Cadence Total Ankle System
Orthopedic
24d
Cleared
Jun 23, 2020
CUSA Clarity Ultrasonic Surgical Aspirator System
Neurology
90d
Cleared
Dec 02, 2019
Integra TITAN Reverse Shoulder System
Orthopedic
270d
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