Kwaliteit & Naleving
Structured systems, validated outcomes, and defined accountability — across every stage of manufacturing.
Audit-Ready Execution: Beyond Marketing Claims
The Daily Evidence Chain of Medical QMS Compliance
In the medical device manufacturing industry, the gap between marketing claims and actual factory execution is often exposed during on-site audits.
At WAKELIFE, compliance is not a certificate on the wall—it is an unbreakable chain of daily evidence.
Cross-Functional Quality Culture
Quality is a company-wide mandate, not just a QA department task.
Quality responsibility at WAKELIFE extends beyond the QC department. From engineering to the assembly line, every team member strictly adheres to Standard Operating Procedures (SOPs). This cross-functional accountability ensures quality is built into the product, not just inspected at the end.
The Unbreakable Evidence Chain
Real daily execution logs, not overnight audit preparations.
True quality management cannot be fabricated overnight. We rely on real-time ERP data and a closed-loop tracking system. Every production log, CAPA report, and batch record is continuously accumulated, making our daily execution impossible to fake.
Medical-Grade Execution Baseline
Exceeding standard requirements with strict ISO 13485 naleving.
We apply ISO 13485 medical device quality standards to all production lines, regardless of the product tier. By maintaining this medical-grade baseline, we guarantee 100% alignment with our OEM/ODM clients’ most stringent QA requirements.
Always Audit-Ready
We invite unannounced on-site validations from professional clients.
Because our documentation reflects actual daily operations rather than rushed audit preparations, our facility remains in an “Audit-Ready” state every single day. We welcome QA directors and compliance officers to verify our manufacturing excellence in person.
WAKELIFE’s manufacturing operations are governed by a structured ISO 13485–aligned quality management system, ensuring that production activities are executed within defined procedures rather than individual discretion.
This system establishes how processes are documented, monitored, and continuously improved across the manufacturing lifecycle—supporting consistency, traceability, and regulatory readiness for medical-grade red light therapy devices.
Quality requirements are embedded into operational workflows, enabling manufacturing outcomes to be guided by standardized controls rather than ad-hoc adjustments.
- Oversight mechanisms ensure system implementation alignment.
- Medical-Grade QMS: ISO 13485 & MDSAP Certified Facility
01 — The Framework
Quality Management System
Production activities are executed within defined procedures rather than individual discretion.
Medical-Grade Manufacturing for Premium Wellness Devices
Proudly ISO 13485 & MDSAP Certified.
We manufacture your red light therapy masks and panels to the world’s strictest medical device quality standards — so you can sell with confidence in every market.
One Audit. Five Countries. Zero Compromise.
Our facility holds MDSAP (Eén auditprogramma voor medische hulpmiddelen) certification — the highest level of manufacturing compliance recognition in the global medical device industry.
| Regulatory Body | Land |
|---|---|
| FDA (Food & Drug Administration) | Verenigde Staten |
| Health Canada | Canada |
| ANVISA | Brazil |
| MHLW / PMDA | Japan |
| TGA (Therapeutic Goods Administration) | Australië |
Zero compliance risk
your products are backed by manufacturing infrastructure already accepted by the world's most stringent regulatory bodies.
Future-proof supply chain
whether you're launching a wellness brand today or seeking FDA/CE medical device clearance tomorrow, our factory is ready.
Full traceability
every component, every batch, every shipment is documented and traceable end-to-end.
WAKELIFE’s quality management system is supported by defined verification and testing capabilities that ensure manufacturing outcomes are validated rather than assumed.
In-House Environment
Our in-house testing environment enables performance consistency, functional stability, and production readiness to be assessed throughout the manufacturing process.
Integrated Workflows
Verification activities are integrated into production workflows, allowing quality requirements to be evaluated continuously—from component integration through final assembly.
"This structured approach ensures that manufacturing decisions are informed by measurable validation rather than subjective judgment."
02 — The Validation
Verification & Testing Capability
We don’t just assemble devices; we validate them. Our core equipment testing ensures that every unit bearing your brand name meets strict medical-grade standards.
Validated Outcomes
Not Assumed Performance
Integrating Sphere
Spectral Analysis System
Technical Standard
Verifies emitted wavelength strictly within a ±5nm tolerance. We test every batch, never just relying on LED datasheets.
Eliminates wavelength uncertainty. Guarantees your end-users receive authentic, medical-grade light therapy rather than standard LED illumination, elevating your brand’s clinical credibility.
Climate Chamber
Extreme Environment Simulation
Test Parameters
Range: -20°C to +60°C
Humidity: 95% RH
Ensures flawless operation across diverse global climates. Whether shipping to cold Nordic regions or humid Southeast Asia, internal components remain protected against environmental stress.
Drop Tester
Structural Integrity Test
Impact Specs
Height: 1.2m
Methode: 6 angles, marble floor impact.
Simulates real-world accidental drops to ensure the housing remains intact and internal circuits stay connected. This directly minimizes after-sales returns (RMA) and protects your brand reputation.
Salt Spray Tester
Corrosion Resistance Test
Exposure Time
24h – 48h continuous salt fog exposure.
Specifically tests against facial sweat and cosmetic residue. Prevents oxidation and poor contact on charging pins and metal parts, significantly extending the product’s lifespan.
Battery Aging Cabinet
Cycle Life Testing
Performance Goal
Capacity > 80% na 500 laadcycli.
Prevents premature battery degradation. Sustaining high capacity after hundreds of uses ensures a premium, long-lasting experience that aligns with high-end beauty brand standards.
- Not What We Say
“Advanced testing equipment”
“Large-scale laboratory”
“State-of-the-art facilities”
- What It Means
Outcomes are validated, not assumed
Decisions are measurable, not subjective
The system is actually executed
Quality is the Best Business Plan
We invite all our OEM/ODM partners to visit our Shenzhen facility and witness these rigorous
ISO 13485 testing procedures in person.
03 — The Recognition
Regulatory Certifications
WAKELIFE’s regulatory certifications reflect the practical implementation of its quality management system across manufacturing operations.
“These certifications are not standalone achievements but indicators of structured quality practices and validated manufacturing discipline.”
FDA nee. (3033883954)
Certificaten uitgegeven door de VS. Food and Drug Administration is te vinden op de Officiële FDA -website.
ISO 13485 / MDSAP
ISO 13485 is een kwaliteitsbeheersysteemstandaard voor gebruik in de regelgevende omgeving van de medische apparaten.
TGA / WEER
De therapeutische goederen administratie (TGA) is de regelgevende instantie voor therapeutische goederen zoals medicijnen, Medische hulpmiddelen en diagnostische tests in Australië.
Ul
Independent safety certification supporting electrical safety compliance and trusted market acceptance.
MDL
De licentie van de Canadese medische hulpmiddelen (MDL) is gelijk aan de VS. FDA's 510(k) goedkeuring.
FCC
FCC -certificering is een verplichte certificering van elektronische producten in de Verenigde Staten.
CE
De CE -markering betekent dat de verkoper verklaart dat zijn product voldoet aan de vereisten van Europese voorschriften.
BSCI
De BSCI -certificering is een zakelijke sociale standaardcertificering die is ontworpen om ervoor te zorgen dat de prestaties van de sociale verantwoordelijkheid van een bedrijf in wereldwijde supply chains voldoet aan internationale normen.
ROHS
ROHS -certificering is een verplichte norm die is vastgesteld door de wetgeving van de Europese Unie. De volledige naam is de “Beperking van richtlijn voor gevaarlijke stoffen.”
Ukca
UK conformity marking supporting compliance with applicable UK product safety and regulatory requirements.
IEC60601
IEC 60601 is een reeks normen ontwikkeld door de International Electrotechnical Commission (IEC).
ISO9001
ISO9001 verwijst naar een certificeringsnorm van kwaliteitsmanagementsysteem ontwikkeld door de International Organisation for Standardization (ISO).
ISO14001
ISO4001 Certificering van het milieubeheersysteem is een standaard voor milieubeheersysteem uitgegeven door de Internationale Organisatie voor Standaardisatie (ISO).
ISO45001
ISO 45001 is een standaard voor gezondheidszorg en veiligheidsbeheersysteem gepubliceerd door de International Organisation for Standardization (ISO).
Oprichtingscertificaat
Dit is het registratiecertificaat van het moederbedrijf Sungrow van Wakelife in Hong Kong.
04 — The Accountability
Quality Governance & Leadership
"This structured approach ensures that manufacturing decisions are informed by measurable validation rather than subjective judgment."
Responsibilities for quality management and compliance are clearly assigned, enabling system implementation to be monitored, maintained, and continuously aligned with regulatory expectations.
This governance approach reflects how regulated manufacturing environments operate—where quality outcomes are shaped not only by processes, but by structured leadership and responsibility.
The Complet Quality Logic
Who Oversees the System?
Learn how quality and compliance responsibilities are defined and overseen across WAKELIFE’s manufacturing operations.