Media
MedTech Signal in the media
Press mentions, interviews and the media kit for MedTech Signal. Journalists and producers can reach us any time at info@mdsignal.org.
Press mentions
Published coverage and public posts about MedTech Signal — each entry links to the original.
- Cross-border regulatory updates: what FDA and Health Canada records show this week
Alignable — Rubicon Microproducts
24 October 2026
A public post introducing MedTech Signal's weekly, source-linked review of FDA and Health Canada regulatory records, with the platform's data-coverage caveats stated up front.
Interviews
No published interviews yet — this section will list them with links as they appear. We are happy to talk with press, podcasts and industry panels about cross-border medical-device regulation and how teams track it. Topics we can speak to:
- Following a device across the US–Canada border: what FDA and Health Canada records can and cannot tell you.
- Why match claims need careful labels — Matched, Possible match, No apparent match — and links to the regulator source.
- What 510(k), recall and QMSR inspection records reveal about device quality trends.
- Building regulatory monitoring for small and mid-sized device companies.
Interview requests: info@mdsignal.org — please include your outlet and deadline.
Media kit
Downloadable brand assets. Please do not recolor, stretch or otherwise alter them, and use the name “MedTech Signal” (two words) in coverage.
Logo mark (SVG)
Brand shield in the primary teal, transparent background. Use for articles and slides.
Download
App icon (PNG)
Square icon used across the product and as the favicon.
Download
Social share image (JPG)
The open-graph card used when MedTech Signal pages are shared.
Download
Company boilerplate
MedTech Signal is a regulatory intelligence platform from Rubicon Microproducts Inc. that turns published regulator records — U.S. FDA 510(k) authorizations, recalls and enforcement data, Health Canada MDALL licences, UK MHRA safety notices and EU EUDAMED certificates — into searchable, source-linked monitoring for medical-device teams.
MedTech Signal is a regulatory intelligence platform for medical-device teams, built by Rubicon Microproducts Inc. in Mississauga, Canada. It organizes published regulator records — U.S. FDA 510(k), De Novo and PMA authorizations, recall and enforcement data, Health Canada MDALL licences, UK MHRA safety notices and EU EUDAMED certificates — into searchable, source-linked monitoring with cross-border company and device matching. Every statement links back to the original regulator record, and match claims are labelled conservatively as Matched, Possible match or No apparent match — the platform never asserts that a device is unlicensed. MedTech Signal is not regulatory advice; it helps teams find the records they need to verify.
Company facts
- Product
- MedTech Signal — regulatory intelligence for medical devices
- Operated by
- Rubicon Microproducts Inc.
- Head office
- 223 Webb Drive, Suite 2803, Mississauga, ON L5B 0E8, Canada
- Media contact
- info@mdsignal.org
- Website
- mdsignal.org
MedTech Signal is operated by Rubicon Microproducts Inc. — see rubiconmp.com for the company behind it.