Life Sciences & Cleanroom LED Lighting
Engineered from the ground up for contamination-controlled environments — ISO3 through ISO8 cleanroom rated with zero particle generation.
Lighting That Protects What You’re Building
In an ISO 5 pharmaceutical cleanroom, a single particle-shedding fixture can compromise a production batch worth millions. cleanLED is engineered around contamination control — not borrowed from a commercial product line.
Particle generation
Zero-particle operation — no thermal cycling debris, no degrading gaskets, no mechanical shedding.
VOC outgassing
Chemical-resistant, non-outgassing materials selected specifically for semiconductor and sterile-fill compatibility.
Ceiling-grid teardrop gaps
Continuous silicone gasket perimeter seals to the ceiling grid — unbroken barrier from cleanroom to plenum.
Maintenance breaches
Above-ceiling service architecture — no tools, parts, or technicians enter the classified space.
Classification range
Rated ISO 3 through ISO 8 — from semiconductor lithography down through medical-device assembly and food processing.
Service intervals
50,000+ hour rated life delays the first maintenance event by years, minimizing requalification cycles.
Engineered for Contamination-Free Environments
ISO Classification Coverage
cleanLED fixtures meet the requirements of ISO 14644-1 cleanroom classifications from ISO 3 through ISO 8 — covering the full range of life sciences, pharmaceutical, and semiconductor environments.
The most stringent classification. Required for advanced semiconductor lithography and nanotechnology fabrication where molecular-level contamination affects device performance.
Required for semiconductor wafer processing and advanced microelectronics assembly where sub-micron particle control is essential for product yield.
The standard for pharmaceutical aseptic fill operations and sterile compounding. FDA and EU GMP regulations require ISO 5 conditions during critical manufacturing steps.
Common for pharmaceutical packaging, biotech laboratory work, and medical device sub-assembly where controlled conditions protect product integrity.
Standard classification for pharmaceutical non-sterile manufacturing, medical device assembly, and biotech research environments requiring controlled conditions.
Entry-level cleanroom classification for food processing, general pharmaceutical operations, and controlled environments that require better than normal room conditions.