Book a 15-minute call with Roberto or Weston, or request a live demo where we bring the device to you. Short platform demos are in production and coming soon. Pick the path that fits how you evaluate technology for your practice.
Choose how you want to evaluate. Each path respects your time: self-serve when you want it, a real conversation when you are ready.
Short platform demos of WAVi, TM-Flow, Max Pulse, ALTMS, and Hue Light are in production. Book a call or request a live demo in the meantime.
See it live on a call →Direct line to Roberto or Weston. We walk you through devices, reimbursement, and onboarding for your specialty.
Pick a time →In-person across California, Nevada, and Arizona. For larger engagements, we travel nationally and internationally; travel costs are quoted separately. Virtual screen-share anywhere else. We bring the device; you bring the questions.
Request a slot →Short demos of WAVi, TM-Flow, Max Pulse, ALTMS, and Hue Light are in production. In the meantime, book a 15-minute call or request a live demo and see each platform run with your own questions on the table.

EEG and event-related potentials in about twenty minutes. FDA 510(k) cleared as an aid in diagnosis. The brain half of baseline, treat, retest.
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Autonomic, sudomotor, and ankle-brachial index in one ten-minute visit. FDA-cleared technologies in one device.
Book a live walkthrough →
Chairside pulse-wave screening with an immediate report. A cardiovascular check, not a replacement for a formal cardiac workup.
Book a live walkthrough →
Transcranial magnetic stimulation, FDA cleared for major depressive disorder. Document against a baseline and prove the change with a retest.
Book a live walkthrough →
Whole-body photobiomodulation under FDA General Wellness scope. Cash-pay positioning, not FDA cleared.
Book a live walkthrough →Pick a time directly on Roberto's or Weston's calendar. No commitment past the first conversation. We get specific about your specialty, reimbursement, and what onboarding actually looks like. You leave knowing whether TITN fits, either way.
Which platforms map to your patient mix, and how baseline, treat, retest applies to your protocols.
Typical CPT codes and reimbursement ranges from EOB data, with the honest "varies by payer" caveat.
Implementation, training, and the white-glove support model so the device actually gets used.
Prefer email or phone? roberto@transitionitnow.com · (213) 444-6123. Pacific Time, call or text.
In-person demos run across California, Nevada, and Arizona, within about six hours of Santa Monica. For larger engagements, we travel nationally and internationally; travel and on-site logistics are quoted separately. Everywhere else, we run a live virtual screen-share of real scans and reports.
In-person within about six hours of Santa Monica across California, Nevada, and Arizona. For larger engagements, we travel nationally and internationally; travel and on-site logistics are quoted separately.
A live screen-share walkthrough of real scans and reports. Same depth, no flights required.
Support across the US, Puerto Rico, Dominican Republic, Mexico, and Central America.
One short form for any of the three paths. Tell us what you want to see and we route it to the right person. This is a wireframe placeholder; the live form connects to TITN's CRM.
The questions we hear most before the first call, answered straight.
No. The first conversation is to figure out fit. BMTG MCI and TBI Reports are available as standalone deliverables, no device purchase needed.
The TITN Support Assistant is online 24/7, built from real support cases for TM-Flow, WAVi, and Max Pulse. It walks you through the common fixes and hands anything bigger to the team.
Each cleared diagnostic maps to its CPT path, standard codes or an unlisted panel code billed per CMS guidance. Ranges we quote are typical from EOB data and vary by payer, plan, and locality. We walk through your specifics on the call.
In-person demos run across California, Nevada, and Arizona, within about six hours of Santa Monica. For larger engagements, we travel nationally and internationally; travel and on-site logistics are quoted separately. Everywhere else, we run a live virtual screen-share of real scans and reports.
Yes. We offer bilingual support across the US, Puerto Rico, Dominican Republic, Mexico, and Central America. Call, email, or submit the form in either language.
Roberto or Weston, not a faceless rep. You get the founder's read on whether the technology fits your practice and your patients.
Start with the Research page. Every device claim traces to the FDA 510(k) database and the manufacturer's studies. Then book a call when you are ready.
Every device named on this page traces to a live FDA 510(k) record or the manufacturer's own regulatory positioning. Reimbursement ranges are typical from EOB data and vary by payer, plan, and locality.
FDA 510(k) K213900, cleared as an EEG and event-related potential system to aid in diagnosis. FDA 510(k) record · WAVi research
LD Technology, three FDA 510(k) clearances in one workstation: K173696 (ankle-brachial index), K152216 (sudomotor), and K200141 (autonomic and HRV). LD Technology studies
FDA 510(k) K110374, a plethysmograph for noninvasive pulse-wave measurement. FDA 510(k) record
REMED Co., Ltd., FDA 510(k) K220625, transcranial magnetic stimulation for major depressive disorder. FDA 510(k) record
Whole-body photobiomodulation positioned under FDA General Wellness scope, not FDA cleared. Hue Light USA
Look up any clearance by K-number in the FDA Premarket Notification database. FDA 510(k) search
Whether you book a call this week or request a live demo, the first step is the same: a clear, honest look at technology that lets you show patients exactly what changed.