Carl Zeiss, Inc. - FDA 510(k) Cleared Devices
44
Total
44
Cleared
0
Denied
Carl Zeiss, Inc. has 44 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 44 cleared submissions from 1980 to 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Carl Zeiss, Inc. Filter by specialty or product code using the sidebar.
44 devices
Cleared
Nov 14, 2001
VISULAS 532S
General & Plastic Surgery
30d
Cleared
Feb 22, 2001
VISULAS YAG II
General & Plastic Surgery
69d
Cleared
Mar 20, 2000
IOLMASTER
Ophthalmic
166d
Cleared
Jan 29, 1999
OPMI TWINER SURGICAL MICROSCOPE
General & Plastic Surgery
88d
Cleared
Apr 23, 1997
SURGICAL MICROSCOPE NAVIGATOR (SMN) SYSTEM/SURGICAL TOOL NAVIGATOR (STN) SYSTEM
Neurology
121d
Cleared
Mar 17, 1997
CPC PROBE
General & Plastic Surgery
341d
Cleared
Jun 21, 1996
HUMPHREY OCT SCANNER
Radiology
88d
Cleared
Nov 24, 1995
HUMPHREY FIELD ANALYZER (HFA II)
Ophthalmic
80d
Cleared
Aug 14, 1995
VISULINK 900 ARGON
Ophthalmic
52d
Cleared
Mar 29, 1995
ZEISS ENDOLIVE STERO ENDOSCOPE
General & Plastic Surgery
26d
Cleared
Sep 28, 1994
ZEISS OPMI L STEREO-LAPAROSCOPE
Obstetrics & Gynecology
553d
Cleared
Jul 01, 1994
MKM (MULTIPLE COORDINATE MANIPULATOR) SYSTEM
General & Plastic Surgery
53d
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