Medical Device Manufacturer · US , Dublin , CA

Carl Zeiss Meditec, AG - FDA 510(k) Cleared Devices

45 submissions · 44 cleared · Since 2004

45

Total

44

Cleared

0

Denied

FDA 510(k) cleared devices by Carl Zeiss Meditec, AG General & Plastic Surgery ✕

5 devices

1-5 of 5

Cleared Oct 25, 2018

General & Plastic Surgery · 181d

Cleared Mar 17, 2010

MODEL VISULAS 532S LASER WITH THE VITE OPTION

General & Plastic Surgery · 70d

Cleared Sep 21, 2007

General & Plastic Surgery · 14d

Cleared Dec 22, 2006

HORUS LASER KERATOME

General & Plastic Surgery · 136d

Cleared Sep 09, 2004

VISULAS YAG III

General & Plastic Surgery · 31d