Multi-format sports nutrition · OEM / ODM for active brands
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ABOUT MITEYO

A Premier Turnkey OEM/ODM Development Partner for Sports Nutrition Brands.

Miteyo (Shenzhen) Biotechnology Co., Ltd. is a cGMP-certified and FDA-registered contract manufacturer specializing in high-growth active nutrition formats: Sublingual Oral Strips, Functional Gummies, Portable Stick Packs, and Precision Powders. We bridge the gap between innovative formulation concepts and mass-market execution. Our in-house R&D team provides complete turnkey OEM/ODM services—from active ingredient encapsulation and flavor masking to custom packaging and full export documentation. Backed by rigorous batch-level quality control (including full COA issuance and heavy metal testing), flexible low MOQs, and rapid 3–7 day sampling, Miteyo empowers sports nutrition and active-lifestyle brands to scale efficiently across specialized categories like Pickleball, Golf, Esports, and Yoga performance lines.

A Premier Turnkey OEM/ODM Development Partner for Sports Nutrition Brands.
OUR ROLE

Turn a market opportunity into a production-ready product brief.

MITEYO works between the buyer’s commercial objective and the technical requirements of product development. We begin with the target consumer, market, sales channel, serving expectation, preferred format, packaging direction and launch plan.

From there, we help organize the questions that determine whether a concept can become a credible product: Can the intended active amount fit into the selected format? Is the serving practical? What flavor and texture direction is realistic? What packaging and documentation will the project require?

Our role is not to force every inquiry into a fixed catalog. It is to help the buyer identify a workable development route before unnecessary sampling, artwork or purchasing decisions are made.

DEVELOPMENT PROGRAMS

A development route matched to the buyer’s launch stage.

Ready-to-Brand (Private Label):
Select from our library of clinically validated base formulas, confirmed flavor systems, and in-stock packaging options. Ideal for sports brands seeking rapid 3–7 day sampling, lower MOQs, and immediate market entry with reduced complexity.

Semi-Custom Execution:
Adjust selected formula elements, key active dosages, custom flavor profiles, or packaging around a reviewed base platform. This route balances swift turnaround time with stronger brand differentiation.

Full Custom ODM Development:
Bespoke formulation engineering built from scratch. Our in-house R&D team supports complex active micro-encapsulation, advanced taste-masking, specialized ingredient sourcing, and complete batch quality/compliance testing.

cGMP CERTIFIED FACILITY

Real Production Capacity & Quality-Control Evidence

Our automated production line is built to handle high-volume OEM/ODM orders with absolute batch-to-batch consistency. Operating under strict cGMP standards, our daily capacity exceeds 10 million units across specialized lines for Sublingual Oral Strips, Functional Gummies, Portable Stick Packs, and Powder Tubs.

• Automated Strip & Pouch Packaging: Dust-free cleanroom environment ensuring zero humidity contamination.
• In-House Analytical Testing: Batch-level heavy metal, dissolution, and micro-viability quality control.
• Flexible Outer Packaging: Supporting custom bottles, outer boxes, foil barrier bags, and multi-serving cartons.

HOW WE WORK

Clear decisions before commercial production.

1. Product brief

Confirm the target consumer, market, format, serving direction, packaging preference, estimated first order and launch timing.

2. Feasibility review

Evaluate whether the requested ingredient amounts, serving count, sensory target and package can work together.

3. Formula and flavor direction

Define the ingredient specification, active load, sweetness, flavor, color, texture and other relevant product requirements.

4. Sampling and evaluation

Produce samples against the reviewed brief and record the changes required before approval.

5. Testing and documentation scope

Confirm the specifications, testing arrangements, label-information inputs and buyer documentation required for the project.

6. Packaging approval

Review package type, serving count, label area, barrier requirements and approved artwork.

7. Commercial production

Begin production after the relevant formula, sample, packaging and commercial conditions have been approved.

8. Export support

Coordinate the confirmed shipping and export-document requirements for the order.

QUALITY APPROACH

Project-Specific Evidence Instead of Generic Promises

Quality requirements should be strictly aligned with your specific formula, target region, and commercial order volume. We provide project-level transparency so your brand can launch with absolute regulatory confidence.

Depending on your confirmed project scope, our quality documentation includes:
• Raw Material Specifications & Allergen Declarations
• Finished Product Specifications & Master Batch Records
• Batch-Level COAs with Mandatory Heavy Metal & Microbiological Testing
• Complete Supply Chain Traceability & Export Labeling Support

Miteyo does not treat generic certificate logos or unsupported statements as a substitute for real quality assurance. Every facility credential, test method, and analytical report is verified and issued specifically for your production run.

WHO WE WORK WITH

Built for buyers with a real product and channel objective.

MITEYO primarily works with sports nutrition brands, fitness and wellness businesses, outdoor and endurance brands, pickleball, tennis and golf businesses, gyms, clubs, recovery centers, private-label retailers and distributors.

We are especially relevant to businesses that:

• Already sell powders or capsules and want to add a consumer-friendly gummy format
• Have an existing sports or active-aging product line and need a portable extension
• Need to compare gummies and powders against a realistic serving target
• Want clearer alignment between formula, packaging, testing and commercial positioning
• Have a defined target market, sales channel, budget direction and launch plan

The most productive project begins with a clear consumer, serving objective, preferred format, estimated first order and target launch date.

CERTIFICATIONS & TESTING

Global Compliance Standards & Mandatory COA Verification

We eliminate import risks and compliance friction for global supplement distributors. Our manufacturing facilities hold full international accreditations, ensuring rapid customs approval across NA, EU, APAC, and Middle East markets.

• Certified Facility: cGMP, FDA-Registered, BRCGS (A-Grade), ISO 22000, and Halal Certified.
• Mandatory Batch Testing: Full Certificate of Analysis (COA) issued for every production batch.
• Heavy Metal & Contaminant Screening: Independent lab verification for Lead, Arsenic, Cadmium, Mercury, and microbial limits.

GLOBAL EXHIBITIONS & PARTNERSHIPS

Building Long-Term Partnerships Through Direct Communication and Practical Solutions

We regularly showcase our newest OEM/ODM formulation breakthroughs at major global trade exhibitions, including SupplySide West, Vitafoods Europe, and FIBO.

These direct interactions allow us to discuss custom active delivery platforms, review flavor and texture samples in person, and align manufacturing roadmaps with international brand managers and buyers.

Whether meeting at global expos or welcoming partners to our cGMP manufacturing facility in Shenzhen, we prioritize transparent technical communication and long-term collaborative growth.

START A PROJECT

Tell us what you want to launch.

Send the market, format, target serving and first-order estimate. We will respond with the most practical development route.

Additional project details

All additional project details are optional.

Privacy information

Your contact details and project brief are stored in the website inquiry system and processed through the existing inquiry email notification service so MITEYO can review and respond. The submission includes the source page, referrer and campaign information when present; a protected IP identifier is used for abuse prevention. Please avoid sending sensitive personal information.

What happens after you submit: feasibility review → questions / reference options → sample route → commercial quote.

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