DISTRIBUTION INTAKE

Put a product in front of us.

Northwest MedTech carries a short card of medical technologies across Oregon, Washington, Idaho, and Alaska. A few lanes are taking new manufacturer relationships right now. Check the board below, then send the intake form — we reply when the product and the lane line up.

01 · STATUS BOARD

What’s open on the card.

Three lanes are taking inquiries; one is closed while a review runs. Sending the form doesn’t create a distribution relationship or a commitment either way — it starts a read on fit.

NW·01 Open

Lane 01 · Medical & health technology

Devices, platforms, and workflow tools

Legally marketed devices, health platforms, and workflow tools for care delivery, monitoring, or quality of life. Routed through qualified provider, clinic, and institutional channels across the footprint.

Submit an inquiry
NW·02 Open

Lane 02 · Neuromodulation & non-opioid pain

Evidence-backed pain devices

Technology aligned to provider-led pathways, approved indications, and firm claims boundaries — no unsupported outcomes language, no off-label promotion. Placed through pain practices, surgery centers, and specialty clinics.

Submit an inquiry
NW·03 Open

Lane 03 · Rehabilitation & recovery

Functional recovery and adherence tools

Tools for functional recovery, movement, and measurable program support. Routed through compliant channels, with workflow fit and provider appropriateness confirmed before anything activates.

Submit an inquiry
NW·04 Under review

Lane 04 · Spine & interventional

Spinal, interventional, and surgical-support devices

Devices for spine, interventional, and surgical-support settings — surgery centers, interventional pain practices, and hospital channels with credentialing and clinical support in place.

A review is running on kyphoplasty and vertebral augmentation. This lane stays closed to new submissions until it concludes.
02 · WHAT TO HAVE READY

Four blocks the form asks for.

Bring enough for us to read the fit. Incomplete submissions don’t get reviewed, and we don’t work off verbal commitments or assumed distribution authority.

Block 01

Product & regulatory

Product name, manufacturer legal name, category, FDA classification and status, intended use, indications, cleared labeling, and a short evidence summary.

Block 02

Commercial model

The distribution structure you propose (commission, wholesale, drop-ship), territory expectations, exclusivity position, training needs, and target launch timing.

Block 03

Target market

Primary provider type, the care settings you’re after, any current Northwest presence, and your near-term channel objectives.

Block 04

Compliance readiness

Complaint and adverse-event routing, recall procedure, current product-liability coverage, and any pending FDA actions or open regulatory items.

MANUFACTURER INTAKE

Send a product in for a read.

Fill every section — partial submissions don’t get reviewed. We reach back only if the product clears the initial read. Sending this creates no distribution relationship, commitment, or agreement.

Keep these out of the form:
  • Patient names, medical record numbers, or any protected health information
  • Adverse-event reports or open FDA safety communications
  • Confidential product files, trade secrets, or pre-submission regulatory documents
  • Inquiries for lanes currently under review or already contracted
Spine and interventional is currently under review for kyphoplasty and vertebral augmentation and is not accepting additional applications.

Submission does not create a distribution relationship, appointment, or agreement. Northwest MedTech will respond only if the product meets the initial review criteria. All fields marked * are required.

BEFORE YOU SEND

Want the fit criteria first?

The manufacturer page lays out what we take on and what we pass, in more detail than the board above — worth a read before the form, or just email us.