Capabilities

Cleanroom Manufacturing

UFP Technologies has manufacturing plants that are ISO 13485 certified and FDA registered, and which house multiple ISO Class 8 and ISO Class 7 cleanrooms and controlled environments.

UFP Technologies has manufacturing plants that are ISO 13485 certified and FDA registered, and which house multiple ISO Class 8 and ISO Class 7 cleanrooms and controlled environments. Within these facilities we utilize HEPA air flow systems to eliminate particulate and perform bioburden testing to ensure low microbial levels.

Our certified cleanroom and controlled environment facilities are equipped to fabricate an array of medical-grade foams, films, and other specialty materials. Our facilities are at the forefront of using advanced processes to launder medical-grade foams and other materials for cleanroom and critical application use.

Cleanroom Locations

Location  ISO Class 8 ISO Class 7
Rancho Dominguez, CA  1
Chicopee, MA  2  2
Georgetown, MA  3
Newburyport, MA  3
Grand Rapids, MI  3
 El Paso, TX  1

Within our cleanroom and controlled environment facilities we have the following capabilities:

UFP Technologies utilizes these capabilities to manufacture custom components, products and packaging for some of the world’s leading medical device and orthopedic implant manufacturers.

Man Walking Through Cleanroom manufacturing of medical devices

Contact Us

Or Give Us A Call At 800-372-3172 To Discuss Your Next Project