







Our laser systems and services are designed with medical device manufacturing in mind, supporting both FDA and EU regulatory requirements.
Compliant with FDA CDRH standards (21 CFR 1040.10 & 1040.11)
Class 1 laser enclosures with safety interlocks and emergency stops
Technical documentation available for audit support
Debris-free, sealed systems suitable for ISO Class 7/8 cleanrooms
Optional recipe tracking, barcode scanning, and validation support (IQ/OQ)
Want to learn more?
Complete the form, tell us which system you’re interested in, and one of our specialists will contact you to discuss your application.