Integra Lifesciences Production Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Integra Lifesciences Production Corporation - FDA 510(k) Cleared Devi...
Recent clearances: Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology, Codman Libertís™ 1.5 mm EVD Catheter with Bactiseal® and Endexo® Technology with Luer Connection (821761), CereLink ICP Monitor (826820), CereLink ICP Extension Cable (826845)
9
Total
9
Cleared
0
Denied
Integra Lifesciences Production Corporation has 9 FDA 510(k) cleared medical devices. Based in Mansfield, US.
Latest FDA clearance: Jun 2026. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Integra Lifesciences Production Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Integra Lifesciences Production Corporation
9 devices
Cleared
Jun 23, 2026
Codman® Distal Peritoneal Catheter, Barium Open End (82-1682)
Neurology
89d
Cleared
Aug 08, 2025
Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology
Neurology
267d
Cleared
Aug 06, 2025
Codman Libertís™ 1.5 mm EVD Catheter with Bactiseal® and Endexo® Technology...
Neurology
264d
Cleared
Feb 04, 2024
CereLink ICP Monitor (826820), CereLink ICP Extension Cable (826845)
Neurology
139d
Cleared
Jan 17, 2024
Bactiseal Catheters
Neurology
90d
Cleared
Dec 19, 2023
Bactiseal EVD Catheter Sets
Neurology
60d
Cleared
Feb 01, 2023
Certas Plus Programmable Valves
Neurology
93d
Cleared
Oct 14, 2022
Hakim Programmable Valves, Hakim Precision Fixed Pressure Valves
Neurology
112d
Cleared
Apr 30, 2021
CereLink ICP Monitor
Neurology
28d