MedTech Signal

Pricing

One workspace, priced by how much of the record you need

Every tier reads the same published FDA and Health Canada records, refreshed on a daily and weekly schedule, with each field linked back to the regulator page it came from. Tiers differ in how many regulators and modules your team can work across.

Every new workspace starts with a 14-day free trial — no card needed. The trial includes Canadian licences, devices, recalls, watchlists and the full alert feed for up to 3 users. Start your free trial.

Essentials

Single-market teams monitoring Canadian licences and recalls

$2,990/ year

USD, per workspace. Equals $249 per month.

SubscribeOr start a 14-day free trial — no card needed
  • Health Canada MDALL licences, devices and identifiers, with active and archived states preserved
  • Health Canada recall records with device links labelled Confirmed, Probable, Possible or No apparent match
  • Watchlists for devices, licences and companies
  • Alert feed with severity, unread tracking and per-category email digests
  • Browser and mobile push notifications, including sound and badge for critical alerts
  • Source links back to the originating regulator record on every screen

Up to 5 users. Daily refresh for licences and recalls.

Professional

Regulatory and market teams working across the US and Canada

$8,990/ year

USD, per workspace. Equals $749 per month.

SubscribeOr start a 14-day free trial — no card needed
  • Everything in Essentials
  • FDA 510(k), De Novo and PMA authorizations, searchable by pathway, product code and decision date
  • FDA ↔ Canada company matching with scored evidence and persistent review decisions
  • Device-level cross-border candidates, including the US devices with no apparent Canadian match view
  • FDA and Health Canada recognized standards side by side, with a change timeline
  • Standards portfolio impact against your watchlists

Up to 25 users. Role-based access: Admin, Member and ReadOnly.

Enterprise

Quality, compliance and strategy groups that need the full record

$24,990/ year

USD, per workspace. Equals $2,083 per month.

SubscribeOr start a 14-day free trial — no card needed
  • Everything in Professional
  • QMSR enforcement: FDA inspection citations, published observations and warning letters, kept distinct across Pre-QMSR and QMSR-era inspections
  • Controlled QMSR finding taxonomy with deterministic mapping and a manual review workflow
  • AI / SaMD evidence benchmark: cohort comparison, CSV export and provenance on every extracted value
  • Evidence review queue for confirming machine-extracted values
  • Administrative controls over data sources, refresh jobs and organization access
  • Single sign-on with Microsoft Entra ID (planned)

Unlimited users. Named onboarding contact.

Subscriptions are sold by Rubicon Microproducts Inc. through our payment provider, who is the merchant of record and handles invoices, taxes and refunds. Questions: info@rubiconmp.com.

What each tier includes

CapabilityEssentialsProfessionalEnterprise
Health Canada licences, devices, identifiersIncludedIncludedIncluded
Health Canada recalls and device linksIncludedIncludedIncluded
Watchlists, alerts, push notificationsIncludedIncludedIncluded
FDA authorizations (510(k), De Novo, PMA)—IncludedIncluded
FDA ↔ Canada company and device matching—IncludedIncluded
Recognized standards and change timeline—IncludedIncluded
Standards portfolio impact—IncludedIncluded
QMSR enforcement and finding taxonomy——Included
AI / SaMD evidence benchmark and review——Included
Data source and job administration——Included
UsersUp to 5Up to 25Unlimited

Coverage is limited to what each regulator publishes. FDA publishes only part of its inspection record, AI/SaMD study values are machine-extracted and review is recommended, and cross-border relationships are candidates for your review — never a statement that a device is unlicensed.

Pricing questions

How does the 14-day free trial work?

Create an account and your workspace starts a 14-day free trial right away — no card needed. The trial includes Canadian licences, devices, recalls, watchlists and the full in-app alert feed for up to 3 users. When it ends, your data stays and you pick a plan to keep going; push notifications need a paid subscription.

How do I subscribe?

Pick a plan, create your account, and pay by card in the checkout window. Access to the modules in your plan starts as soon as the payment is confirmed.

What counts as a user?

Anyone with a sign-in to your workspace. Each user holds one access level: Admin (data sources, refresh jobs and review workflows), Member (intelligence, watchlists, alerts and comparisons) or ReadOnly (view only).

How is billing handled?

Monthly or annual, per workspace, in USD. Rubicon Microproducts Inc. sells through a payment provider who is the merchant of record and issues your invoice, applies any sales tax or VAT, and processes refunds. Manage your card, invoices or cancellation from Billing inside the app.

Can we cancel?

Yes, from the Billing page at any time. Your workspace keeps full access to the end of the period you have already paid for. Refund requests within 30 days of a charge are handled by our payment provider.

Can we change tier later?

Yes. Moving up takes effect immediately and adds the modules to your existing watchlists and alerts. Moving down keeps your data and hides the modules that are no longer part of your plan.

Is the data real-time?

No. Sources refresh on a schedule — licences and recalls daily, authorizations, standards and enforcement weekly — and every screen shows the last successful refresh for the source behind it.

Is any of this regulatory advice?

No. MedTech Signal organizes records published by regulators and links back to the original source. Confirm anything you rely on against the linked regulator record.

Subscribe and start monitoring

Create your workspace, add the devices, licences and companies you already track, and see what each scheduled refresh reports. Cancel from the Billing page any time.

Subscribe