Ensuring Quality Standards in Our Products and Processes
ISO 13485:2016
A quality management system standard that specifies the requirements for regulatory purposes for medical devices. UL Certificate # 35765.230523 (Exp. Date May 2026)
FDA Registration # 3026544741
A regulatory process to ensure the safety, efficacy, and quality of various products marketed in the United States.
cGMP Compliant Systems
Consistent production and quality control of products, mainly in pharmaceuticals, biotech, and medical devices.
CFR 820
This certification indicates that the manufacturer follows FDA regulations and has established a reliable quality system to ensure their products are safe and effective.
UL REGISTERED FIRM
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