Clean Room Converting Services
ISO Class 8 certified clean room converting for medical devices, electronics, semiconductor, and aerospace applications. ISO 13485 certified and FDA-registered facility.
Overview
ALS Tape operates ISO Class 8 (Class 100,000) certified cleanroom converting facilities covering tens of thousands of square feet. The facility is ISO 13485 and ISO 9001:2015 certified and FDA-registered. Converting operations include precision rotary die cutting, in-line multi-layer lamination, island placement, inline pouching, slitting, packaging, and kitting — all performed within the controlled environment. Achievable tolerances reach ±1/32 inch for precision-critical applications. Clean room converting is suited to medical devices, in-vitro diagnostics, wearable sensors, electronics assemblies, semiconductor components, aerospace parts, and battery components where particulate control is required.
Process Options
Precision rotary die cutting within ISO Class 8 cleanroom environment.
In-line multi-layer lamination for complex adhesive and film stack constructions.
Island placement for precise component positioning on liner or carrier.
Inline pouching for sealed, contamination-protected component delivery.
Slitting, packaging, and kitting performed without leaving the controlled environment.
Supported Materials
Medical-grade adhesive tapes and transfer films
Functional and protective films for electronics
Semiconductor process tapes and liners
Foam and elastomer materials for medical and wearable applications
Typical Applications
Medical device and diagnostic adhesive components
Wearable sensor and continuous monitoring patches
Electronics and enclosure clean-room bonding parts
Semiconductor substrate and process-critical tape components
Aerospace and battery assembly adhesive parts
Material Groups and Delivery Support
Related Products
Related Industries
FAQ
What cleanroom certification level does the converting facility hold?
The facility is certified to ISO Class 8 (Class 100,000) and holds ISO 13485 and ISO 9001:2015 certifications. The facility is also FDA-registered.
What tolerances can clean room converting achieve?
Precision rotary die cutting within the cleanroom can achieve tolerances of ±1/32 inch for medical, electronics, and contamination-sensitive applications.
What types of converting operations are performed in the cleanroom?
Rotary die cutting, multi-layer lamination, island placement, inline pouching, slitting, packaging, and kitting can all be performed within the cleanroom without leaving the controlled environment.
Which industries commonly require clean room converting?
Medical devices, in-vitro diagnostics, wearables, consumer electronics, semiconductor components, aerospace assemblies, and EV battery applications are common clean room converting users.
Need a Converting Partner?
Clean Room Converting Services
Share your drawing, dimensions, material preferences, or downstream assembly requirements. ALS Tape can help align fabrication methods with delivery format.