Ellipse A/S - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Ellipse A/S has 7 FDA 510(k) cleared medical devices. Based in Hoersholm, DK.
Historical record: 7 cleared submissions from 2007 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ellipse A/S Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Ellipse A/S
7 devices
Cleared
Mar 26, 2020
Ellipse Frax 1940 for Ellipse Nordlys and Ellipse Ydun
General & Plastic Surgery
157d
Cleared
Mar 15, 2018
Ellipse Ydun
General & Plastic Surgery
29d
Cleared
Sep 16, 2016
Frax 1550 for Ellipse Nordlys/ Ellipse Nordlys+, Ellipse Sirius, Ellipse...
General & Plastic Surgery
144d
Cleared
Jul 07, 2015
Ellipse Nordlys/Ellipse Nordlys+, Ellipse Sirius, Ellipse Infinity, Ellipse...
General & Plastic Surgery
95d
Cleared
Sep 25, 2014
ELLIPSE I2PL+/ELLIPSE MULTIFLEX+
General & Plastic Surgery
191d
Cleared
Oct 17, 2008
ELLIPSE MULTIFLEX
General & Plastic Surgery
151d
Cleared
Sep 12, 2007
ELLIPSE JUVIA, MODEL 9EJU7465
General & Plastic Surgery
51d