7136 Gettysburg Pike   |   Fort Wayne, IN 46804 - USA

Product Availability and Regulatory Status

BioPoly, LLC is committed to bringing the BioPoly RS systems to the United States and International countries. At present, these devices are CE marked for use in most international markets and seeking IDE approval for use in the United States.

Education & Training

  • BioPoly LLC is conducting surgeon training for the BioPoly RS Knee, Patella, and Shoulder system in select countries.  
  • Contact us for information on the next training opportunity.

Visiting Surgeon Program

  • Additional Visiting Surgeon Program (VSP) information coming soon!

Clinical Use

  • Patients are receiving the BioPoly implants throughout Europe and parts of Asia.
  • In the UK, patients are being enrolled in a multi-centre post-market registry study for the BioPoly Patella Implant.  Click here to learn more.
  • A BioPoly Knee and Patella specific pathway has been launched on Amplitude to allow clinicians to collect clinical outcomes from their patients. Instructions for using the pathway can be found in the Amplitude Pro One User Guide.

Intended Use

BioPoly® RS Knee System
   Cartilage lesion located in weight bearing region of medial or lateral femoral condyles or the                   trochlear facets

BioPoly® RS Patella System
   Cartilage lesion located in medial or lateral facets of the patella

BioPoly® RS Shoulder System
   Cartilage lesion located in humeral head

Device Description

The BioPoly® RS Partial Resurfacing Knee, Patella, and Shoulder Implants are long term, surgically invasive devices for replacement of focal osteochondral defects.

Contact Us We can help you answer any questions you may have about BioPoly.

Get in touch!

Packaging and Sterilization

The BioPoly® RS Partial Resurfacing implants are provided sterile and for single use.

Adverse Effects

Infections, allergies, or other reactions to implant materials.