FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LenSx Laser System (8065000944)

K Number: K252682 · Decision Sep 24, 2025
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
46
Applicant Total
43
Review Days
30

Basic Information

Device Name
LenSx Laser System (8065000944)
K Number
K252682
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alcon Laboratories, Inc.
Date Received
August 25, 2025
Decision Date
September 24, 2025
Product Code
OOE
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OOE Ophthalmic Femtosecond Laser

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Other Clearances by Alcon Laboratories, Inc.

K Number Device Name
K254052 DAILIES TOTAL1®; DAILIES TOTAL1® Multifocal
K243896 LenSx Laser System (8065998162)
K243909 Precision1; Precision1 for Astigmatism; Dailies Total1; Dailies Total1 for Astigmatism; Dailies Total1 Multifocal; Dailies Total1 Multifocal Toric
K242184 Alcon 27GA Chandelier (8065000252); Alcon 27+ DS Wide Angle Endoilluminator (8065000253); Alcon 27+ DS Endoilluminator (8065000256);
K233876 UNITY VCS (8065000296); UNITY CS (8065000297)
K233902 Centurion™ Vision System (Active Sentry™) (8065753057)
K233856 Precision1; Precision1 for Astigmatism; TOTAL30; TOTAL30 for Astigmatism; TOTAL30 Multifocal
K232921 DAILIES TOTAL1®; DAILIES TOTAL1® Toric; DAILIES TOTAL1® Multifocal; DAILIES TOTAL1® Multifocal Toric
K230785 Precision1, Precision1 for Astigmatism
K222500 AIR OPTIX COLORS
Search all 43 clearances from Alcon Laboratories, Inc. →