Back In Motion Group
- Shockwave Therapy
- Arthritis Treatment
- Erectile Dysfunction (ED) Treatment
Read the Shockwave Therapy guide for the educational context behind this treatment category.
Brooklyn, NY
If you are looking for shockwave therapy and EMTT in Brooklyn, confirm that the office offers both and explains why each fits your diagnosis. Shockwave uses acoustic energy, while extracorporeal magnetotransduction therapy, or EMTT, uses pulsed magnetic fields. Some Brooklyn practices advertise them together, but a shockwave listing alone does not establish EMTT availability or a reason to combine them. Expect only some offices on this list to offer both devices, so check each listing rather than assume every clinic provides the combination.
Local options include chiropractic and rehabilitation offices in Borough Park, Park Slope, and Carroll Gardens, rather than a single treatment district. The area around Thirteenth Avenue in Borough Park and the Court Street corridor in Carroll Gardens are places to check when comparing office addresses. Fourth Avenue connects the Park Slope side of this search with Sunset Park and routes toward Borough Park. Confirm the treatment address, subway access, and stairs or elevator arrangements, especially if heel or knee pain makes repeated trips difficult.
Expect an office consultation covering symptoms, previous treatment, medications, and an examination before a clinician recommends a device. Ask whether a physician, physical therapist, chiropractor, or another licensed professional evaluates you, who operates the equipment, and who supervises care. Request the manufacturer and exact device, whether it delivers focused shockwaves or radial pressure waves, and written information about discomfort, bruising, and other risks. Agree on how follow up will assess walking, work, or exercise goals and what happens if symptoms persist. If both are proposed, ask whether they are billed together or separately, and how the quote changes if you choose only one.
Shockwave and EMTT services are often cash pay, so request a quote separating the evaluation, each device treatment, rehabilitation, and follow up. Evidence varies by diagnosis, and evidence for adding EMTT remains limited; many marketed uses are not FDA approved, even when a device has authorization for another purpose. Ask what regulatory indication applies to the proposed device and your condition. The national shockwave therapy hub explains the mechanisms and evidence across treatment uses.
Regenerated.com is free for patients, and organic listing order is not sold. Featured placements are labeled and capped; Verified reflects credential checks, not spending. Directory inclusion is not an endorsement of a provider or its proposed care. For help comparing entries, read How to read a Regenerated city hub and Featured vs Verified vs organic.
Regulatory context
FDA 510(k) clearances exist for specific extracorporeal shockwave devices indicated for chronic plantar fasciitis and lateral epicondylitis. Shockwave lithotripsy for kidney stones is approved under 21 CFR 876. LI-ESWT is not FDA-approved for erectile dysfunction in the United States as of 2026, and no shockwave device is FDA-cleared for knee osteoarthritis, Peyronie's disease, cellulite, or sexual wellness indications. Off-label use by licensed practitioners is permitted, but marketing implying FDA approval for those uses is not and is subject to FDA, FTC, and state enforcement.
The New York State Education Department's Office of the Professions oversees medical, chiropractic, and physical therapy licensure, while the Office of Professional Medical Conduct (OPMC) investigates physicians. The New York Attorney General applies GBL 349 aggressively to deceptive health advertising and has a history of pursuing regenerative medicine and men's health clinics for unsupported claims. New York City and Long Island have been particular enforcement hotspots. Shockwave clinics advertising ED treatment as FDA-approved face elevated exposure. Regenerated.com listings in New York should reflect accurate FDA-clearance status and avoid approval language for off-label uses.
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