Quick-Med Technologies, Inc. - FDA 510(k) Cleared Devices

Quick-Med Technologies, Inc. is a materials chemistry and microbiology company headquartered in Gainesville, Florida. Founded in 1997, the company develops antimicrobial textile technologies designed for hygiene and infection control applications. Quick-Med specializes in sustainable, green antimicrobial solutions for consumer, industrial, and medical markets, with global production and distribution capabilities.

The company has received 1 FDA 510(k) clearance from 2 total submissions. Quick-Med's regulatory activity spans from 2009 to 2013, with its cleared device in the General & Plastic Surgery category. The company is currently inactive in the FDA 510(k) database, with no submissions recorded in the past decade, and should be treated as a historical regulatory record.

Quick-Med's primary FDA 510(k) cleared device was a skin fold management textile designed for general hospital use. The company's core technology platform addresses antimicrobial resistance through biomimetic coatings applied to textiles, including collaborations with the U.S. Air Force on pathogen-resistant airplane seating. Products marketed under the Stay Fresh brand have been incorporated into consumer apparel and medical applications.

Explore the company's complete FDA 510(k) submission history, device names, product codes, and clearance dates in the database records below.