8 yrs
Shaved off TransMed7's development cycle
End-to-End Manufacturing Partner
The supplier that got you through prototyping can't always scale with you. Fictiv carries your parts history, DFM notes, and quality documentation (including AS9100D and ISO 13485:2016 capabilities) from first article through full-scale production.
8 yrs
Shaved off TransMed7's development cycle
10M+
Parts manufactured through Fictiv’s platform
3-6 months
Saved by eliminating mid-program supplier re-qualification
Re-qualifying a new production supplier mid-program costs 3–6 months—and that's before the first article cycle.
Say goodbye to messy handoffs. Your CAD files, finalized DFM notes, material certifications, and supplier performance data all live in a single accessible platform. When you're ready to scale, nothing starts over.
Review Specs with Expert >FAIR, PPAP, CoC, material certs—Fictiv's quality system supports full production documentation requirements. Whether you're submitting to the FDA, the FAA, a prime contractor, or an enterprise customer, the paperwork is in the platform.
Consult a Quality Engineer >Fictiv's global network scales with your volume. AI-driven sourcing routes your orders to the right supplier at every production tier—without you having to find them.
Request a Platform Demo >| . | Re-Qualifying a New Supplier |
|---|---|
| Timeline impact | 3-6 months lost in timeline |
| First article cycle | Restart from scratch |
| Quality documentation | Re-generate all records |
| FDA / regulatory readiness | Re-validate supplier |
| Engineering overhead | High—new RFQs and DFM, new relationships |
| Volume scalability | Fixed or uncertain |
| Zero—program context carries forward |
| Builds on existing parts history |
| On demand in platform |
| ISO 13485:2016 & AS9100D capable network, pre-qualified |
| Low—single platform, single team |
| Flexible—US, Mexico, India, China network |
8 years faster
Millions saved
Zero qualification overhead
"Fictiv enabled us to shave 8 years off of the product development timeframe for our first two devices. Fictiv enabled us to save millions of dollars in infrastructure, people and time costs when compared to traditional development and supply chain strategies."
Dr. James Vetter
Co-Founder & CMO, TransMed7
What happens when I need to scale from prototype to production?
Do I really need multiple vendors for prototyping and production?
Can Fictiv provide inspection reports, material certifications, and certificates of conformity (CoCs)?
How can I reduce part costs without redesigning everything?
How is Fictiv different from local shops or traditional contract manufacturers?
Will I need to re-qualify suppliers when production volume increases?