Somatex Medical Technologies GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Somatex Medical Technologies GmbH - FDA 510(k) Cleared Devices
Recent clearances: Tumark Vision, Tumark Professional, Tumark Q, Tumark Professional Q-Shape, Tumark for Eviva, Tumark for Brevera, Tumark Vision
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) Regulatory Record - 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