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. 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 demos of WAVi, TM-Flow, Max Pulse, ALTMS, and Hue Light are being produced now. Book a live walkthrough in the meantime.
Book a live walkthrough →Roberto or Weston takes the call personally. We walk you through devices, reimbursement, and onboarding for your specialty.
Pick a time →A one-hour slot, in person across California or by live screen-share anywhere else. For larger engagements we travel nationally and internationally; travel costs are quoted separately. We bring the device; you bring the questions.
Book the demo →Short demos of WAVi, TM-Flow, Max Pulse, ALTMS, and Hue Light are in production. Book a live walkthrough now 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, not to diagnose any condition on its own. The brain half of baseline, treat, retest.
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Autonomic, sudomotor, and ankle-brachial index in one ten-minute visit. Built on three FDA 510(k)-cleared modules.
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Chairside pulse-wave screening with an immediate report. A cardiovascular check, not a replacement for a formal cardiac workup.
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Transcranial magnetic stimulation, FDA cleared for major depressive disorder. Document against a baseline and prove the change with a retest.
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Whole-body photobiomodulation under FDA General Wellness scope. Cash-pay positioning, not FDA cleared.
Book a live walkthrough →Pick a time on the TITN calendar below, or reach Roberto or Weston by phone, text, or email. 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.
Your contractor's policy, the coverage checklist, and the one page worksheet, with the honest "decided by your payer" caveat.
Implementation, training, and the white-glove support model so the device actually gets used.
In-person demos run across California. 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. The demo is a one-hour slot on the TITN calendar.
In-person across California. 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 email for any of the three paths. Tell us what you want to see and we route it to the right person.
TITN and BMTG reach attorneys through education only. The ordering provider is the customer. The report does not diagnose; it documents measured data a clinician interprets, and admissibility is determined by the court.
The questions we hear most before the first call, answered straight.
No. The first conversation is to figure out fit. BMTG Cognitive Function and Post-Injury Brain Function 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.
Coverage is decided by your payer on the documented indication. We quote no reimbursement figure; on the call we walk through your contractor's policy, the coverage checklist, and the one page worksheet, and your certified coder confirms every code.
In-person demos run across California. 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. TITN publishes no reimbursement figure; coverage is decided by the payer.
FDA 510(k) K213900, cleared as an EEG and event-related potential system to aid in diagnosis, not to diagnose any condition on its own. FDA 510(k) record · WAVi research
TM-Flow System, built on three FDA 510(k)-cleared LD Technology modules: 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.