Mesh, Surgical, Deployer — FDA 510(k) Devices
Intended To Be Used To Facilitate The Delivery Of Soft Tissue Prosthetics During The Laparoscopic Repair Of Soft Tissue Defects (e.g. Hernia Repair).
1
Total
1
Cleared
54d
Avg days
2025
Since
List of Mesh, Surgical, Deployer devices cleared through 510(k)
1 devices
How to use this database
This page lists all FDA 510(k) submissions for Mesh, Surgical, Deployer devices (product code ORQ). Click any device to view full submission details, including the decision date, manufacturer information, predicate device, and a link to the official FDA record.
These devices fall under the Orthopedic FDA review panel. Browse all Orthopedic devices →