End-to-End Manufacturing Partner

One Partner.
Prototype to Production.
No Re-Qualification.

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

Your prototype supplier got you parts.
But they may not get you to market.

Re-qualifying a new production supplier mid-program costs 3–6 months—and that's before the first article cycle.

No Re-Qualification.
Your Program Context Carries Forward.

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 >

Production Documentation,
Ready When You Are.

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 >

Same Partner from
10 Parts to 10,000.

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 >

The Fictiv advantage

. 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
fictiv logo
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
"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

FAQs

What happens when I need to scale from prototype to production?

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Do I really need multiple vendors for prototyping and production?

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Can Fictiv provide inspection reports, material certifications, and certificates of conformity (CoCs)?

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How can I reduce part costs without redesigning everything?

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How is Fictiv different from local shops or traditional contract manufacturers?

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Will I need to re-qualify suppliers when production volume increases?

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Your Prototype Is Proven. Now Scale It.

ISO 13485:2016-Capable AS9100D-Capable FAIR PPAP CoC Full Material Traceability