Medical Device Manufacturer · DK , Hoersholm

Ellipse A/S - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2007

Recent clearances: Ellipse Frax 1940 for Ellipse Nordlys and Ellipse Ydun, Ellipse Ydun

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Ellipse A/S General & Plastic Surgery ✕

7 devices

1-7 of 7

Cleared Mar 26, 2020

Ellipse Frax 1940 for Ellipse Nordlys and Ellipse Ydun

General & Plastic Surgery · 157d

Cleared Mar 15, 2018

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