OptiLight™

GUDID 07290109145280

LUMENIS LTD.

Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system
Primary Device ID07290109145280
NIH Device Record Keyeaaab725-4dab-4999-84d1-e520265a3ef8
Commercial Distribution StatusIn Commercial Distribution
Brand NameOptiLight™
Version Model NumberOptiLight™
Company DUNS600166524
Company NameLUMENIS LTD.
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 Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107290109145280 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-08-02
Device Publish Date2021-07-25

Devices Manufactured by LUMENIS LTD.

07290118853701 - Lumenis Pulse 60H, 60Hz2023-12-18
07290109144924 - Stellar SapphireCool LG 6mm2023-08-16
07290109144931 - Stellar SapphireCool LG 15x352023-08-16
07290109144948 - Stellar SapphireCool LG 8x152023-08-16
07290109146676 - SurgiTouch Scanner 2022-09-30
07290109146133 - UltraPulse® DUO2022-09-28 UltraPulse DUO
07290109147055 - VersaPulse PowerSuite 80/100W2022-09-27
07290109147062 - VersaPulse PowerSuite 80/100W2022-09-27

Trademark Results [OptiLight]

Mark Image

Registration | Serial
Company
Trademark
Application Date
OPTILIGHT
OPTILIGHT
97363371 not registered Live/Pending
Lumenis Be Ltd.
2022-04-14
OPTILIGHT
OPTILIGHT
90673899 not registered Live/Pending
Lumenis Ltd.
2021-04-27
OPTILIGHT
OPTILIGHT
79287995 not registered Live/Pending
Pilkington Group Limited
2020-01-31
OPTILIGHT
OPTILIGHT
79215665 5393754 Live/Registered
Pilkington Group Limited
2017-04-24
OPTILIGHT
OPTILIGHT
76229014 not registered Dead/Abandoned
Zenfinity Inc.
2001-03-22
OPTILIGHT
OPTILIGHT
75366986 not registered Dead/Abandoned
POLY-OPTICAL PRODUCTS, INC.
1997-10-02
OPTILIGHT
OPTILIGHT
75087413 2106447 Dead/Cancelled
OPTILIGHT, INC.
1996-04-12

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.