Somatex Medical Technologies GmbH - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Somatex Medical Technologies GmbH has 7 FDA 510(k) cleared medical devices. Based in Cambridge, US.
Last cleared in 2021. Active since 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Somatex Medical Technologies GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Somatex Medical Technologies GmbH
7 devices
Cleared
Feb 18, 2021
Tumark Vision, Tumark Professional, Tumark Q, Tumark Professional Q-Shape
General & Plastic Surgery
227d
Cleared
Oct 31, 2018
Tumark for Eviva, Tumark for Brevera
General & Plastic Surgery
90d
Cleared
Mar 22, 2018
Tumark Vision
General & Plastic Surgery
30d
Cleared
Nov 08, 2011
TUMARK FLEX FOR MAMMOTOME,TUMARK FLEX FOR ATEC
General & Plastic Surgery
145d
Cleared
Jun 24, 2011
BIOPSY HANDY, MRI BIOPSY HANDY
Gastroenterology & Urology
273d
Cleared
Feb 17, 2010
TUMARK PROFESSIONAL, MODEL 271560, MR-TUMARK PROFESSIONAL, MODEL 601560
General & Plastic Surgery
140d
Cleared
Mar 19, 2008
TUMARK PROFESSIONAL, MODEL 271560
General & Plastic Surgery
139d