BUYER'S GUIDE · Updated October 15, 2026

SoftWave vs StemWave: Shockwave for Wellness Clinics (2026)

Both are marketed to chiropractic and wellness clinics. Their regulatory paths differ, which affects what you may claim in marketing.

Provisional: this is an initial research list built from vendor websites (checked October 15, 2026). We have not tested these products hands-on, and we do not publish a numeric score until we have verified pricing and specs against the rubric. Anything we could not verify says “not verified yet”. Ask vendors for written quotes and specs.

FDA status

• SoftWave OW100S:Used in Dr. Goss’s practice
  Dr. Goss’s take (personal opinion)

  “SoftWave is the shockwave system I use in my practice. Its patented applicator is FDA-cleared for specific uses, and it’s become one of the most dependable tools in my clinic. In my experience, it’s taken our clinical outcomes to the next level.”

  — Dr. Ryan Goss, DC

  510(k)-cleared (K213120) for minor muscle aches and pains, temporary increased local circulation, and activation of connective tissue; also cleared (K231710) for chronic diabetic foot ulcers and second-degree burns with standard care. SoftWave clearances
• StemWave Modus-F: Class I therapeutic massager, 510(k)-exempt; registered and listed, which StemWave notes is not clearance or approval. Intended use: temporary relief of minor muscle aches and pains and temporary increased circulation. StemWave regulatory statement

Business questions

• Device price, financing and any per-treatment or subscription fees (not verified).
• Territory or exclusivity terms and marketing support.
• Keep marketing claims within the cleared or listed intended use.

FAQ

Is SoftWave FDA approved?

It is FDA 510(k)-cleared for specific indications, which is different from approval.

Is StemWave FDA cleared?

StemWave says its device is Class I, 510(k)-exempt and FDA-listed, not cleared or approved.