Paige Maness

Paige Maness is responsible for all activities related to regulatory and quality compliance. Paige has over twelve years experience in the medical device industry straddling quality assurance and regulatory affairs and has worked with a variety of devices from class I instruments to class III spinal implants to software-only medical devices.

She obtained her Master's in Archives and Public History at NYU, and her thesis was published in The Journal of Archival Organization. She is considered one of the few experts on Bertillonage, which indulges her passion for forensic science.