FAQ
Quick answers to common questions.
All products and procedures comply with applicable FDA regulations and are manufactured in cGMP facilities. Indications vary — we discuss compliant options during consult.
Most protocols include an initial treatment and scheduled follow‑ups. Your personalized plan is based on condition, biomarkers, and goals.
Yes. We coordinate with your care team and provide detailed summaries and outcomes tracking.
Candidacy depends on diagnosis, severity, and medical history. Contraindications may include active infection, uncontrolled bleeding disorders, or pregnancy. We screen for suitability during consult.
Many patients report incremental improvements over 2–12 weeks as tissue remodeling and signaling occur. Timelines vary by condition and protocol.
Yes, image guidance is recommended for precise placement in joints, tendons, or soft tissue. It may be included or added depending on indication.
Typical effects include temporary soreness, swelling, or stiffness at the injection site. Most resume light activity within 24–48 hours; detailed aftercare is provided.
Durability depends on diagnosis, biomechanics, and adherence to rehab. Some protocols include booster sessions or adjunct therapies for sustained benefit.
We follow applicable regulations and use cGMP‑sourced products where appropriate. We provide research summaries and safety data during consult.
Pricing depends on the protocol; HSA/FSA may apply. We can provide receipts and flexible packages; financing options are available for some services.
Procedures are performed by licensed clinicians with appropriate training and oversight, typically in an office/clinic setting using sterile technique.
Pre‑procedure guidance may include hydration, medication adjustments, and activity planning. Aftercare includes activity progression, icing/heat guidance, and follow‑up check‑ins.