Genesys Orthopedics Systems, LLC

One device in the database

  • Model / Serial
    The devices being recalled have a catalog number of G826 and a lot number of 11406.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Nationwide Distribution including NV, CA, NY, MO, TX, FL, NJ, GA, TN.
  • Product Description
    Circular Lock Screws, part # G826, lot # 11406. The Lock Screws are part of the Genesys Spine TiLock Pedicle Screw System. || The TiLock Pedicle Screw System is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of thoracic, lumbar, and sacral spine: degenerative disc disease (DDD) (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies); spondylolisthesis; trauma (i.e. fracture or dislocation); spinal stenosis; curvatures (i.e. scoliosis, kyphosis, and/or lordosis); tumor; pseudoarthrosis; and failed previous fusion).

One manufacturer with a similar name

Learn more about the data here

  • Manufacturer Address
    Genesys Orthopedics Systems, LLC, 1250 S Capital of Texas Hwy Ste 600, Bldg # 3, West Lake Hills TX 78746-6446
  • Manufacturer Parent Company (2017)
  • Source
    USFDA