LENSX

GUDID 20380650000549

LENSX SOFTFIT PATIENT INTERFACE NOMINAL,EO

Alcon Laboratories, Inc.

Ophthalmic laser system eyeball positioning suction cup
Primary Device ID20380650000549
NIH Device Record Keyc712f4a2-fcb8-4d13-b1af-b6330593adb1
Commercial Distribution StatusIn Commercial Distribution
Brand NameLENSX
Version Model Number8065000054
Company DUNS008018525
Company NameAlcon Laboratories, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100380650000545 [Primary]
GS120380650000549 [Package]
Contains: 00380650000545
Package: [60 Units]
In Commercial Distribution

FDA Product Code

HQCUnit, phacofragmentation

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-11-14
Device Publish Date2022-11-04

On-Brand Devices [LENSX]

00380659981623LenSx Laser System
10380650000573LENSXPATIENT INTERFACE FLAP 10PK,EO
20380650000563LENSX SOFTFIT PATIENT INTERFACEI FLAT,EO
20380650000556LENSX SOFTFIT PATIENT INTERFACE STEEP,EO
20380650000549LENSX SOFTFIT PATIENT INTERFACE NOMINAL,EO
10380650000535LENSX LASER SOFTFIT PATIENT INTERFACE 10 PK, EO

Trademark Results [LENSX]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LENSX
LENSX
77365935 3670196 Live/Registered
Alcon Inc.
2008-01-07
LENSX
LENSX
77365932 3870850 Live/Registered
NOVARTIS AG
2008-01-07
LENSX
LENSX
77365929 3857264 Live/Registered
NOVARTIS AG
2008-01-07
LENSX
LENSX
73483053 1330917 Live/Registered
BERKSHIRE PAPER CO., INC.
1984-06-01

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