enlighten

GUDID 00816722021625

enlighten SR Laser System

CUTERA, INC.

Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system Dermatological frequency-doubled solid-state laser system
Primary Device ID00816722021625
NIH Device Record Keyfbb02a6d-8c87-4b16-830b-b83e6e126cb6
Commercial Distribution StatusIn Commercial Distribution
Brand Nameenlighten
Version Model Numberenlighten SR
Company DUNS041071643
Company NameCUTERA, 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 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

Customer Support Contacts

Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com
Phone1 415 657-5500
Emailinfo@cutera.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100816722021625 [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 Number2
Public Version Date2018-07-06
Device Publish Date2018-03-02

On-Brand Devices [enlighten]

00816722023605enlighten Micro Lens Array handpiece attachment
00816722021649enlighten III Laser System
00816722021625enlighten SR Laser System
00816722021618enlighten Low Energy Green Laser System
00816722021601enlighten Laser System

Trademark Results [enlighten]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ENLIGHTEN
ENLIGHTEN
98421613 not registered Live/Pending
ENLIGHTEN CANDLES, LLC
2024-02-26
ENLIGHTEN
ENLIGHTEN
97819985 not registered Live/Pending
ENLIGHTEN CANDLES, LLC
2023-03-02
ENLIGHTEN
ENLIGHTEN
90806910 not registered Live/Pending
Kasisto, Inc.
2021-07-01
ENLIGHTEN
ENLIGHTEN
90806857 not registered Live/Pending
Kasisto, Inc.
2021-07-01
ENLIGHTEN
ENLIGHTEN
90700180 not registered Live/Pending
Enlighten Group Pty Ltd
2021-05-10
ENLIGHTEN
ENLIGHTEN
90235767 not registered Live/Pending
Thrive Technologies, Inc.
2020-10-05
ENLIGHTEN
ENLIGHTEN
90004544 not registered Live/Pending
CI Events, LLC
2020-06-16
ENLIGHTEN
ENLIGHTEN
88882884 not registered Live/Pending
Enlighten IT Consulting LLC
2020-04-22
ENLIGHTEN
ENLIGHTEN
88843239 not registered Live/Pending
LEREVE SKIN INSTITUTE INC
2020-03-22
ENLIGHTEN
ENLIGHTEN
88222884 not registered Live/Pending
Silicon Studio Corporation
2018-12-10
ENLIGHTEN
ENLIGHTEN
88000096 5842371 Live/Registered
Connect With Julianna, LLC
2018-06-14
ENLIGHTEN
ENLIGHTEN
87834049 not registered Live/Pending
Enlighten Innovations Inc.
2018-03-14

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