Corporate Film

EYESEO Eye Care OEM/ODM/OBM

Step into the smart supply chain, see quality and strength

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In short: EyeOEM is an eye-care OEM/ODM source factory in Guangzhou, China, certified to ISO 22716 and GMPC (FDA and CPNP registration ready), with 12 automated lines, a Class 100,000 cleanroom and a library of 20,000+ proven formulas. Minimum order quantities are from 500 units for stock formulas and from 3,000 units for newly developed formulas; sampling takes about 7–15 days and mass production about 10–20 days. Both on-site and remote video audits are available by appointment.

Eye-Care Smart Manufacturing

Data-backed strength — the trust foundation for every OEM/ODM partnership.

Factory Video Tour

on siteVideo Library

From raw material to shipment — auditable at every step

EyeOEM under-eye patch OEM promo video
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Under-Eye Patch OEM Promo
EyeOEM skincare production-to-shipment full process, on site
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Full Process: Production to Shipment
EyeOEM automated production line, on site
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Automated Production Line
EyeOEM product showroom, on site
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Product Showroom
20+
Years experience
5000+
Brand clients
20,000+
Formulas
12
Auto production lines
CORE MANUFACTURING STRENGTH

Four Core Competences

Efficient, flexible, scalable smart-manufacturing support for your brand

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Intelligent Manufacturing Base

INTELLIGENT MANUFACTURING

20,000㎡ digital smart eco-park, 100,000-grade GMPC cleanroom, 12 fully automated lines, German IKA homogenizer & smart emulsification, daily filling capacity 100K+.

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R&D Innovation Engine

R&D INNOVATION

Top industry experts lead our core R&D team; in-house modern smart R&D center focused on Eastern skin traits, continuously driving product innovation & upgrades.

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Global Supply Chain Network

GLOBAL SUPPLY CHAIN

Integrating global premium resources, 100+ top raw-material suppliers, direct sourcing of core actives; full-spectrum packaging ecosystem from basic to high-end customization.

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Full-chain Brand Empowerment

BRAND EMPOWERMENT

Beyond traditional OEM — one-stop service from market insight and hero-product planning to marketing support, helping brands break through fast and grow sustainably.

Certifications

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GMPC
Cosmetics GMP
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ISO 22716
Cosmetics QMS
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FDA
US registration
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CPNP
EU notification
CERTIFICATION & QUALITY

20 Years of Smart Manufacturing · Int’l Authoritative Certification

Full-chain standardized quality control — quality that stands up to the world’s strictest inspections

EyeOEM quality testing laboratory — pH titration and spectrophotometric analysis

International Certification System

INTERNATIONAL CERTIFICATION SYSTEM

From incoming materials to finished goods, strict standardized production & testing

  • Awarded US GMPC (Good Manufacturing Practice for Cosmetics) certification
  • Complies with EU EMA pharmaceutical-grade strict regulations
  • Fully meets US FDA drug management standards
  • Certified to international SGS EU-standard system
EyeOEM global export logistics base — container loading and freight trucks ready for dispatch

International Intelligent Manufacturing Base

INTERNATIONAL INTELLIGENT MANUFACTURING BASE

Complete full-lifecycle quality management — safe, efficient, stable from design & mass production to warehousing & shipping

  • German IKA homogenizer & smart emulsification equipment
  • Multi-stage reverse osmosis (RO) + EDI ultra-pure water system
  • Fully automated filling equipment, daily capacity 100K+
  • Factory tours available by appointment — see for yourself
Trusted by EyeOEM global client logo wall

Book a Factory Visit

On-site or video factory tour. See the production lines and quality control yourself.

Buyer FAQ

Certification, compliance and how to verify us

Certification, compliance and supplier verification — the five questions buyers ask before they commit.

What cosmetic manufacturing certifications do you hold?
EyeOEM operates an eye-care production plant certified to ISO 22716:2007 Cosmetics Good Manufacturing Practice (GMPC), covering the full production of eye-care products.
The certification scope covers under-eye patches, eye masks, steam eye masks, eye creams and eye serums.
Certificate copies and annual surveillance audit reports are available on request. On-site or video factory audits are supported, with the production lead walking you through the lines, cleanroom grades and QC process.
Can you help with EU CPNP notification?
Yes. For the EU market, we supply the production-side documentation required for CPNP notification: formulation, label and instruction artwork, finished-product test reports, and we support the Responsible Person with the Declaration of Conformity (DoC) and the production section of the technical documentation.
If your brand does not yet have an EU Responsible Person, we can point EU partners to qualified RP service providers.
Do you support FDA registration and MoCRA compliance for the US market?
Yes. For the US market, we support buyers with the production and compliance documentation needed for FDA cosmetic establishment registration and product listing, and provide the export compliance document pack.
The additional establishment registration and product listing requirements introduced under MoCRA are supported. Where relevant, the submission itself is completed by the brand or its regulatory partner, with the manufacturer supplying the factory-side evidence chain.
How can I confirm you are a factory and not a trading company?
Four checks you can run yourself:
1. Audit — own production lines accept on-site or video audits; traders usually cannot get you into the production floor.
2. Production scheduling — only a factory can put you in direct contact with production scheduling and shift plans.
3. Batch traceability — retained batch samples, inspection records and original release-test archives are available.
4. Legal entity — check whether the business licence and manufacturing licence cover cosmetic manufacturing.
For entity verification we can provide a company registry lookup link containing the Unified Social Credit Code, and production-line livestreams can be scheduled.
What are the MOQ, sampling and mass-production lead times for eye masks and eye creams?
MOQ varies by formula type and cooperation model:
Spot wholesale
· Under-eye patches, eye masks, steam eye masks: 500 units / SKU
· Eye creams and eye serums: from 300 units
· Eye beauty devices: from 100 units
New custom production (after sampling)
· Under-eye patches: 50,000 pairs
· Eye masks and steam eye masks: 10,000 units
· Eye creams and eye serums: 5,000 units
· Eye beauty devices: 1,000 units
Sampling and mass-production lead times depend on formula type, complexity and order size. MOQs and lead times are negotiable.

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Factory Capability and Compliance — Key Parameters

EyeOEM is an eye-care OEM/ODM source factory covering under-eye patches, eye masks, eye creams, steam eye masks and eye beauty devices. The table below lists the hard numbers buyers ask for during supplier screening — every line is verifiable.

All figures reflect actual line configuration, not inflated ranges. For a detailed equipment list or copies of system certificates, email sales@eyeoem.com.

ItemSpecification
CertificationISO 22716, GMPC; FDA and CPNP registration ready
Production lines12 automated lines covering emulsifying, filling and packing
Cleanroom classClass 100,000 cleanroom with pharmaceutical-grade water treatment
Formula library20,000+ proven formulas, adaptable by claim and skin feel
Sampling lead timeAbout 7–15 days depending on formula complexity and packaging
Mass production lead timeAbout 10–20 days depending on order size and packaging availability
MOQFrom 500 units for stock formulas; from 3,000 units for newly developed formulas
Factory auditOn-site and remote video audits available by appointment

Do you handle both ODM and OEM?

Yes. ODM uses our proven formulas and packaging options; OEM produces to your specified formula and packaging. The two can be combined.

Can the ISO 22716 certificate be verified?

Yes. System certificates and test reports ship with the quotation pack, and originals can be checked on site during an audit.

Have you shipped to both the EU and the US?

Yes. For the EU we supply the product information file required for CPNP; for the US we provide facility and product documentation required under MoCRA.

Do you accept small pilot runs?

Yes. Pilot runs from 500 units are accepted for market validation, priced on a different tier than full production.