Demetech Corp. - FDA 510(k) Cleared Devices

Demetech Corp., specializes in surgical sutures and wound closure devices, with a manufacturing facility in Miami, US. The company develops both absorbable and non-absorbable suture products for surgical applications.

Demetech received 10 FDA 510(k) clearances from 10 total submissions, with all devices cleared in the General & Plastic Surgery category. The company's regulatory history spans from 2002 to 2014. Demetech is currently inactive, with no new clearances recorded in recent years.

The company's cleared portfolio includes a range of suture technologies: synthetic absorbable options such as poliglecaprone, polydioxanone, and polyglycolic acid; natural absorbable gut sutures; and non-absorbable varieties including nylon, polyester, silk, and polypropylene. These products serve general and plastic surgical procedures.

Explore the complete list of device names, product codes, and clearance dates in the database.