Demetech Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Demetech Corporation - FDA 510(k) Cleared Devices
Recent clearances: DemeMASK, DemeDIOX Barbed Absorbable Surgical Suture, DemeTECH DemeFORCE Nonabsorbable Surgical Suture
5
Total
5
Cleared
0
Denied
Demetech Corporation has 5 FDA 510(k) cleared medical devices. Based in Miami Lakes, US.
Historical record: 5 cleared submissions from 2018 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Demetech Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Demetech Corporation
5 devices
Cleared
Jul 24, 2020
DemeMASK
General Hospital
50d
Cleared
Nov 07, 2019
DemeDIOX Barbed Absorbable Surgical Suture
General & Plastic Surgery
170d
Cleared
Jul 31, 2019
DemeTECH DemeFORCE Nonabsorbable Surgical Suture
General & Plastic Surgery
127d
Cleared
Oct 11, 2018
DemeTECH PTFE Nonabsorbable Surgical Suture
General & Plastic Surgery
118d
Cleared
Aug 27, 2018
DemeTECH DemeDIOX absorbable surgical suture
General & Plastic Surgery
73d