REONEER REGENERATIVE STUDIO
Your brand,
our regenerative engineering.
Our 18 years of experience in regenerative medicine, combined with our CE-certified T-LAB components, transforms into your signature product. No need for a new CE application. To market in a matter of weeks.
18
Years of Experience
CE
CERTIFIED COMPONENTS
6-12
LAUNCH IN WEEKS
Approach
Studio is more than mass production.
1— SPEED
On the market within weeks.
No CE application required (12–18 months). Our components are already CE-certified. Bring your brand; enter the market with a declaration under the system package model.
2 — FREEDOM
Building blocks like Lego.
5 Microlyzers × 3 tubes × 1 syringe × countless protocols. PRP, PRF, BMAC, SVF, Exosomes, Micrografts, Fat Grafts — components selected from the Reoneer amd T-LAB ecosystem come together in a kit tailored to your vision.
3 — FOR PIONEERS
It's not a standard OEM.
Reoneer operates at the cutting edge of regenerative medicine. Studio is your gateway to this frontier—a dedicated team of regenerative engineers assigned to you.
How does it work?
In five steps, from your desk to the shelves.
The process is transparent, and our commitments are in writing. If we don’t see the right fit, we’ll let you know early on—we respect your time.
01
Write Your Project
10 min
A brief form—who you are, what you need, and what vision you’re working toward.
02
Product Specialist Review
1–2 business days
Our regenerative engineering team will review your proposal and assess its maturity and suitability.
03
Technical Brief + Initial Pricing
About 1 week
We will share with you the component selection, potential architectures, and the initial commercial commitment document.
04
Strategic Zoom
Post-maturity
We’ll sit down with your product owner to discuss the protocol, business model, and timeline.
05
Contract + Production + Launch
6–12 weeks total
Branding, production run, documentation, labeling, launch support. Your brand on the shelves.
WHAT CAN YOU BUILD?
Component palette. Your architecture .
Tubes
Smart Syringe
Blades and Filters
Accessory
Category
Typical application
PRP
Platelet-rich plasma kits — aesthetics, orthopedics, hair.
PRF
Fibrin-matrix-based, sustained-release protocols. Fibrin or injectable form.
BMAC
Bone marrow aspirate concentration — orthopedic applications.
SVF
Stromal vascular fraction — adipose tissue processing. The most advanced level of mechanical application.
Exosome
Autologous exosome preparation protocols
Micrograft
Mechanical micrografting systems — hair, dermal applications.
Fat Grafting
Lipoaspirate purification — orthopedic and aesthetic applications.
Hybrid / Custom
Combining multiple modalities into a single kit.
What could yours be?
“5,000 sets per year for a VIP hair clinic”
“BMAC for an orthopedic distributor”
“Signature Exosome Kit”
An exosome development kit that lets a manufacturer with its own PRP tubes enter the exosome field.
Hybrid for a newly established startup
Who is it for?
We’re selective. Honestly.
Suitable partner
✓ Distributors aiming to become regional leaders
✓ Clinic chains with an annual potential of ≥ 1,000 sets
✓ Innovative startups aiming to create a new category with their signature product
✓ Groups seeking to reduce the number of suppliers while maintaining quality
✓ Physicians who provide training in the regenerative field and need their own custom kits
Not suitable
— Those looking for small, one-time batches
— Institutions that purchase based solely on price
— Early-stage ventures lacking clinical maturity
— The pursuit of speed without certification in non-CE markets
— Projects seeking “the same thing, but cheaper
The figures are finalized based on the project’s maturity. The studio works with each partner individually.
From the workshop notebook
Two anonymous comments.
Europe · Aesthetic chain
The Signature Hair Kit will be available in four markets within eleven months
A multi-location aesthetic group sought to reduce the number of suppliers for hair treatments. The PRP + Micrograft hybrid kit was delivered along with a custom packaging design and a clinical protocol training module. Eleven months after the initial order, the kit is now actively in use across four markets: Germany, Belgium, the United Kingdom, and Spain.
TIER
Signature
Category
PRP + Micrograft
Middle East · Distributor
Private-label SVF — the first in its region.
TIER
Signature
Category
SVF Kit + Custom Design
Application
Write your project. 10 minutes..
The more you share, the more mature our technical brief will be.
Our product specialist will get back to you within 1–2 business days.
Frequently Asked Questions
Five honest answers.
Is this an OEM service?
No. The OEM/private-label model is one-way—you provide the branding, and we handle production. Studio is a two-way process: our regenerative engineering team works with you to design the architecture, refine the protocol, and tailor it to your clinical practice. The product bears your signature; the engineering is a collaborative effort.
Can I sell it without a CE certificate?
Yes—we’re working under the system package model. Our components are already CE-certified; you can bring the product to market as a system package using a kit architecture and through a declaration of conformity. This does not require a separate CE application process (12–18 months). The details will be clarified in the technical brief based on your target market.
Who owns the product?
The brand, packaging design, product name, clinical packaging, and marketing rights belong to you. The technology behind the components and the production line belong to us. This distinction is clearly defined in writing in the contract.
How long does it take?
A typical Signature project takes 6 to 12 weeks from application to launch. The Starter option takes less time, while the Atelier (hybrid/custom protocol) takes longer. The timeline becomes clear once the component selection is finalized.
To which countries can I ship?
The markets we currently operate in are Europe (CE), Turkey, and select Middle Eastern and Gulf countries. For Latin America and Asia, a market-specific regulatory assessment is required; if you specify your target market in your application, we will discuss eligibility first.