Medical Device Manufacturer · US , Cambridge , MA

Somatex Medical Technologies GmbH - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2008
7
Total
7
Cleared
0
Denied

FDA 510(k) cleared devices by Somatex Medical Technologies GmbH General & Plastic Surgery ✕

6 devices
1-6 of 6
Cleared Feb 18, 2021
Tumark Vision, Tumark Professional, Tumark Q, Tumark Professional Q-Shape
K201863 · NEU
General & Plastic Surgery · 227d
Cleared Oct 31, 2018
Tumark for Eviva, Tumark for Brevera
K182082 · NEU
General & Plastic Surgery · 90d
Cleared Mar 22, 2018
Tumark Vision
K180443 · NEU
General & Plastic Surgery · 30d
Cleared Nov 08, 2011
TUMARK FLEX FOR MAMMOTOME,TUMARK FLEX FOR ATEC
K111692 · NEU
General & Plastic Surgery · 145d
Cleared Feb 17, 2010
TUMARK PROFESSIONAL, MODEL 271560, MR-TUMARK PROFESSIONAL, MODEL 601560
K093064 · NEU
General & Plastic Surgery · 140d
Cleared Mar 19, 2008
TUMARK PROFESSIONAL, MODEL 271560
K073095 · NEU
General & Plastic Surgery · 139d
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