Quality & Compliance
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.
ISO 13485 Quality Baseline
Medical-device quality standards across every production line.
We apply ISO 13485-based quality controls across production to support demanding OEM/ODM quality 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 support market-specific compliance preparation based on the exact product, configuration, intended use, and destination market.
MDSAP-Audited Quality System
Shenzhen Sungrow LED Technology Co., Ltd., WAKELIFE’s parent company, has been audited under the Medical Device Single Audit Program (MDSAP) and holds BSI Certificate MDSAP 800873.
Regulatory requirements included in the documented audit scope:
Australia — Therapeutic Goods Administration requirements
Canada — Health Canada medical device requirements
United States — U.S. FDA medical device quality-system requirements
MDSAP is a quality-management-system audit program. It does not by itself approve, clear, license, or authorize a product for sale. Product market status must be verified separately for the exact model, intended use, labeling, and destination market.
Built for Global Compliance
Manufacturing and quality systems designed for major regulated markets.
Future-Ready Supply Chain
Ready to support wellness products today and regulated-market expansion tomorrow.
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
Method: 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% after 500 charge cycles.
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 the testing and quality-control procedures operated within our ISO 13485-certified quality management system.
03 — The Recognition
Regulatory, QMS, Product Compliance & Corporate Records
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 Registration No. 3033883954
Verifiable through the FDA Establishment Registration & Device Listing database on the official FDA website.
ISO 13485 / MDSAP
Medical device quality management systems supporting regulated market requirements.
TGA / SAA
The Therapeutic Goods Administration (TGA) is the regulatory body for therapeutic goods such as medicines, medical devices and diagnostic tests in Australia.
UL
Independent safety certification supporting electrical safety compliance and trusted market acceptance.
MDL
Health Canada MDL for applicable medical devices.
FCC
FCC certification is a mandatory certification of electronic products in the United States.
CE
The CE marking means that the seller declares that his product complies with the requirements of European regulations.
BSCI
The BSCI certification is a Business Social Standard certification designed to ensure that a company’s social responsibility performance in global supply chains meets international standards.
ROHS
RoHS certification is a mandatory standard established by European Union legislation. Its full name is the “Restriction of Hazardous Substances Directive.”
UKCA
UK conformity marking supporting compliance with applicable UK product safety and regulatory requirements.
IEC60601
IEC 60601 is a series of standards developed by the International Electrotechnical Commission (IEC).
ISO9001
ISO9001 refers to a quality management system certification standard developed by the International Organization for Standardization (ISO).
ISO14001
ISO4001 Environmental Management System Certification is an environmental management system standard issued by the International Organization for Standardization (ISO).
ISO45001
ISO 45001 is an occupational health and safety management system standard published by the International Organization for Standardization (ISO).
Certificate of Incorporation
This is the registration certificate of WAKELIFE’s parent company Sungrow 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.
Who Oversees the System?
Learn how quality and compliance responsibilities are defined and overseen across WAKELIFE’s manufacturing operations.
05 — The Traceability
Unit-Level Evidence: From Line to End User
"Every device leaves the line with a verifiable identity — not a label, but a record."
Unit-Level Traceability
Every device is assigned a unique laser-marked ID linked to its production records.
Permanent Unit ID
Unique, durable identification for every device.
ERP-Linked Records
Tracks material batch, production line, QC, and shipment data.
Operational Value for OEM / ODM Partners
— retrieve a unit’s full production record within hours, enabling root-cause analysis instead of batch-wide assumptions.
— export records per unit, batch, or shipment, aligned with MDSAP audit expectations.
— limit corrective action to affected units rather than broad recalls.