Integra Lifesciences Corporation
105 and 109 MORGAN LANE, PLAINSBORO, NJ, US
Registered product codes
9 product codes
Recent MDR events
7,089 on file
- MAYFIELD MODIFIED SKULL CLAMPJul 31, 2026Other3004608878-2026-00083
- Mayfield Composite Series Skull ClampJul 31, 2026Other3004608878-2026-00084
- Unknown Mayfield Skull ClampJul 27, 2026Other3004608878-2026-00079
- MAYFIELD INFINITY SKULL CLAMPJul 27, 2026Malfunction3004608878-2026-00082
- MAYFIELD MODIFIED SKULL CLAMPJul 27, 2026Malfunction3004608878-2026-00080
- Mayfield Composite Series Skull ClampJul 27, 2026Other3004608878-2026-00081
- Unknown BioMendJul 27, 2026Injury2648988-2026-00021
- UNKNOWN MAYFIELD SKULL CLAMPJul 21, 2026Injury3004608878-2026-00076
- MAYFIELD MODIFIED SKULL CLAMPJul 20, 2026Malfunction3004608878-2026-00077
- MAYFIELD SWIVEL ADAPTOR A1018Jul 20, 2026Injury3004608878-2026-00078
Recalls
34 on file
- TerminatedFeb 10, 2015
Through an investigation of complaints, Integra found that there is the possibility for the locking handle mechanism of the Base Units to fail during use.
View FDA record ↗ - TerminatedJun 2, 2014
New Deal has identified through a complaint report that some 3.5 mm Diameter x 22 mm Length Surfix screws in Lot no. F626 (Catalogue No. 285322S) have been packaged and labeled as 3.5mm Diameter x 30 mm Length Surfix screws (Catalogue No. 285330S).
View FDA record ↗ - TerminatedJul 16, 2013
As a result of the investigation into an adverse trend of complaints for reports of misalignment of the calcaneal or tibial screws during use of the Panta Nail Support Device, Integra has decided to issue this voluntary medical device correction. The misalignment can result in the inability to properly insert the screws into the Panta Nail and create the potential need for revision surgery.
View FDA record ↗ - TerminatedMay 10, 2013
Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
View FDA record ↗ - TerminatedMay 10, 2013
Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
View FDA record ↗ - TerminatedMay 10, 2013
Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
View FDA record ↗ - TerminatedMay 10, 2013
Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
View FDA record ↗ - TerminatedMay 10, 2013
Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
View FDA record ↗ - TerminatedMay 10, 2013
Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
View FDA record ↗ - TerminatedMay 10, 2013
Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
View FDA record ↗
Compliance history
Matched by FEI 1121308.
FDA inspections
2 on file
- Official Action Indicated (OAI)Aug 22, 2024
Compliance: Devices
- No Action Indicated (NAI)Aug 22, 2024
Postmarket Assurance: Devices
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
1 on file
Import refusals
0 on file
No import refusals on file for this FEI number.