Medical devices

The surgeon wants it. Value analysis has not heard of you.

We put your ads in front of every name on the committee, clinical, supply chain, finance, and the physician champion, so the approval process does not start from zero.

The problem

Deals die in value analysis, and the loss looks like nothing.

You have a rep network and clinical evidence, and your motion depends on a surgeon or department lead falling in love with the device.

Then it hits value analysis. A committee that has never met you, has no clinical stake, and evaluates on cost, contract compliance and risk. Your champion has to carry you through a process they do not control, armed with a brochure.

Deals die there constantly, and the loss looks like nothing. No rejection, just a meeting that keeps getting rescheduled.

Who has to say yes

The buying committee on this deal

01

Physician or surgeon champion

Wants it, has no budget authority.

02

Value Analysis Committee

The actual gate: clinical, nursing, supply chain, finance.

03

Supply chain or materials management

Cares about GPO contracts and standardization.

04

CFO or VP Finance

Cares about total cost and reimbursement.

05

Biomed or clinical engineering

On anything with a service or integration component.

06

Nursing leadership

Whose workflow changes.

Your rep sees the surgeon. Nobody sees the other five. That is the gap.

What sets it off

The moments that create the deal

A GPO contract coming up for renewalA new service line or facilityA safety event with the incumbent deviceNew clinical evidence publishedA supply chain leader hiredReimbursement changes affecting the procedure

What we do differently here

Built for how this market actually buys

We cannot and will not replace your rep network. What we do is warm the committee around the champion, so when it reaches value analysis, four of the six people have seen your clinical data, your outcomes, and your cost story for months.

On channel and compliance: medical device targeting runs primarily on LinkedIn and programmatic. Platform policy restricts audiences that could suggest health-related information, so Meta plays a limited role here and we are explicit about that upfront. Every claim in every ad goes through your regulatory review before it runs, no exceptions, and we build that into the timeline.

Proof

Real operators. Real outcomes.

AfterSchool HQ

The closest analog in our portfolio. A purchase that required superintendents, technology directors, curriculum heads and finance leads to all agree, a committee structure very close to value analysis. Meetings booked in week one. Seven-figure deal closed within the engagement window.

We will be straight with you on the meeting about what we have and have not proven in medical devices specifically.

Fit

You are a fit if

Device or system sells at $30k+, or as a capital purchase
Sales cycle involves a value analysis or capital committee
You have clinical evidence and regulatory clearance
You have reps who can close when the committee is warm

The rest of the machine

The same system runs behind every vertical we serve

Next step

Get your free Pipeline Diagnostic.

We will map the named buyers in your market, show you what the first 90 days looks like, and tell you plainly if this is not a fit.

Other industries

Book a Pipeline Review