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Device
keratome, ac-powered
Regulation Description
Keratome.
Product Code
HNO
Regulation Number
886.4370
Device Class
1
Premarket Reviews
Manufacturer
Decision
ALLERGAN, INC.
SUBSTANTIALLY EQUIVALENT
2
BAUSCH & LOMB, INC.
SUBSTANTIALLY EQUIVALENT
4
BioVision Technologies, LLC
SUBSTANTIALLY EQUIVALENT
2
CIBA VISION
SUBSTANTIALLY EQUIVALENT
2
HOWARD INSTRUMENTS, INC.
SUBSTANTIALLY EQUIVALENT
3
KERAVISION, INC.
SUBSTANTIALLY EQUIVALENT
1
LASERSIGHT TECHNOLOGIES, INC.
SUBSTANTIALLY EQUIVALENT
3
MILLENNIUM
SUBSTANTIALLY EQUIVALENT
5
MORIA
SUBSTANTIALLY EQUIVALENT
2
OASIS
SUBSTANTIALLY EQUIVALENT
1
SCHWIND EYE-TECH-SOLUTIONS GMBH & CO. KG
SUBSTANTIALLY EQUIVALENT
2
SIS LTD. SURGICAL INSTRUMENT SYSTEMS
SUBSTANTIALLY EQUIVALENT
1
SURGICAL SPECIALTIES CORP.
SUBSTANTIALLY EQUIVALENT
1
Device Problems
No Known Device Problem
159
Normal
79
Contamination during use
43
Not Applicable
16
Other (for use when an appropriate device code cannot be identified)
14
Fire
8
Unknown (for use when the device problem is not known)
6
Suction issue
5
Device Issue
3
Failure to cut
3
Particulates
3
Unintended system motion
2
No Information
2
No code available
2
Optical distortion
1
Material perforation
1
Device damaged prior to use
1
Loss of power
1
Smoking
1
Device stops intermittently
1
Vacuum, loss of
1
Calibration error
1
Component(s), broken
1
Total Device Problems
354
Recalls
2007
2008
2009
2010
2011
2012
2013
Class I
0
0
0
0
0
0
0
Class II
1
1
0
0
2
0
0
Class III
0
0
0
0
0
0
0
Recalls
Manufacturer
Recall Class
Date Posted
1
AMO Manufacturing USA, LLC
II
Nov-04-2011
2
Bausch & Lomb Inc
II
Oct-22-2008
3
Bausch & Lomb Inc
II
Aug-02-2007
4
Wavelight AG
II
May-25-2011
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