We only work with top highest quality allograft products from Signature Biologics
Our process is the most thorough, from the pre-op, the ultrasound guided procedure, and all the way through the regenerative cycle with our follow up system.
We only work with the highest trained professionals to guild your regenerative experience. Our staff or Medical doctors and Nurse practitioners are excited to participate in your success!
REGULATORY AND COMPLIANCE
Signature Biologics’ products are derived only from healthy, pre-screened live C-Section births in the USA.
To ensure patient safety, donor selection and tissue recovery and processing meet or exceed all applicable industry standards.
All products undergo independent sterility testing and are manufactured in a Good Tissue Processing (GTP) facility.
Signature Cord™ and Signature Matrix™ are HCT/P products designed and produced to be in compliance under Section 361 of the Public Health Services Act, 21 CFR Part 1271.10 as a human cell and tissue product for homologous use only.
Signature Cord is derived from dissociated umbilical cord tissue following minimally manipulative procedures. It also is a natural source of growth factors and hyaluronic acid. Our process does not alter the regenerative properties of the umbilical cord, maintaining the integrity of the source material that is required for tissue repair.
We strive to develop novel and unique processes to produce best-in-class products while maintaining a continued focus on research and further product development.We are committed to complying with the highest regulatory standards and conduct all business with a high degree of integrity.
Signature Cord is available in various concentrations
based upon tissue weight.
What is Stem Cell Recruitment Therapy®?
What benefits does Stem Cell Recruitment Therapy® Injections offer?
Powerful Treatment: Helps to relieve pain associated with joints, soft tissue and spinal injuries.
Convenient & Painless: 15-minute in office, single injection.
All Natural & Drug-free: Contains a large concentration of Growth Factors, including bFGF “Basic fibroblast growth factor” – this is a signaling protein encoded by a gene that assists in cell growth and maturation, and tissue repair
Quick & Reduced Recovery Time: Return to everyday, low impact activities.
Safe, Non-steroidal Alternative to Surgery: Helps recruit your body’s stem cells and healing components to reconstruct and regenerate the injured tissue that is causing pain.
Stem Cell Recruitment Therapy® is safe and effective, helping the body boost its ability to heal itself. It is administered through a single injection of Human Amniotic Fluid (AF).
What is an Amniotic Fluid Injection (AF)?
Amniotic Fluid contains a rich mixture of collagen, cytokines, elastins and growth factors that creates an extra-cellular matrix which supports healing and has the potential to reduce scarring and inflammation.
AF is filled with growth factors which assist the body in tissue repair, reducing pain and inflammation and contributing to the regeneration and reconstruction of injured tissue.
Russell Health, Inc. Disclaimer
Stem Cell Recruitment Therapy®, Stem Cell RecruitmentTM(SCR), Stem Cell Recruitment TherapyTM(SCRT), SCR FacialTM, DermaFloTM, OrthoFactorTM and VivadermTM are trademarks of Russell Health, Inc. The treatments described on this marketing are not considered to be standard of care for any condition or disease. The treatments described on this marketing are not considered to be standard of care for any condition or disease. SCR, SCRT, SCR Facial, DermaFlo, OrthoFactor and VivadermTM attempt to utilize acellular, minimally manipulated tissue allografts and are comprised of tissue allograft components intended for homologous use to supplement tissue. Stem Cell Recruitment TherapyTM products are classified by the Food and Drug Administration (FDA) as Human Cell, Tissue and Cellular and Tissue-Based Products (HCT/P) that are regulated solely under section 361 of the Public Health Service (PHS) Act. FDA recognizes that human tissue was designed, or evolved, to perform certain functions in the human body with exquisite safety and effectiveness. As an HCT/P regulated solely under Section 361 of the PHS Act, Russell Health’s Stem Cell Recruitment TherapyTM products are exempt from FDA pre-market review, clearance, and approval from FDA. Please consult your doctor to see if an amniotic fluid injection is right for you. No medical advice has been offered herein. These statements have not been evaluated by the FDA. This product is not intended to diagnose, treat, cure or prevent any disease. Results may vary.
Platelet Rich Plasma
Patients who are not a candidate for surgery but are experiencing day to day pain due to their injury with no significant relief from physical treatment, may be candidates for Platelet Rich Plasma treatment. This could include those with:
- Golfer’s Elbow
- Tennis Elbow
- Achilles Tendonitis
- Rotator Cuff
- Plantar Fasciitis
According to the American Journal of Sports Medicine, patients with chronic elbow tendinosis showed the following results after the PRP injection:
46% pain relief by 4 weeks
60% pain relief by 8 weeks
81% pain relief by 6 months
At the conclusion of the study, 93% of the patients were completely satisfied with the treatment and had avoided surgery.