eMax AS10812

GUDID 07290109950013

eMax System 115VAC

SYNERON MEDICAL LTD

Multi-modality skin surface treatment system
Primary Device ID07290109950013
NIH Device Record Key73f5a32f-33af-498d-a449-cfafe6076603
Commercial Distribution StatusIn Commercial Distribution
Brand NameeMax
Version Model NumberAS10812
Catalog NumberAS10812
Company DUNS532685716
Company NameSYNERON MEDICAL 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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com
Phone1.866.259.6661
Emailinfo@Syneron-Candela.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107290109950013 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-20

Devices Manufactured by SYNERON MEDICAL LTD

07290109952703 - SA Flat Lrg. Repl. Cover 25x50mm, 4Hr, Velashape III 2020-03-31 SA Flat Lrg. Repl. Cover 25x50mm, 4Hr, Velashape III
07290109952857 - Intima Sterile 2 Internal + 1 External HP, Accessories Kit2020-02-10 Intima Sterile 2 Internal + 1 External HP, Accessories Kit
07290109952864 - eTwo System2020-02-10 eTwo System
17290109952724 - Regular Internal Handpiece 5-Pack Sterile Single-Use, CO2RE Intima2020-02-10 Regular Internal Handpiece 5-Pack Sterile Single-Use, CO2RE Intima
17290109952823 - External Handpiece 5-Pack Sterile Single-Use, CO2RE Intima2020-02-10 External Handpiece 5-Pack Sterile Single-Use, CO2RE Intima
17290109950379 - Internal, CO2RE Intima2019-02-07 Internal, CO2RE Intima
07290109950167 - Purple swivel lens2019-02-07 Purple swivel lens
07290109950273 - Lens, Gold & Silver2019-02-07 Lens, Gold & Silver Assy, CO2RE

Trademark Results [eMax]

Mark Image

Registration | Serial
Company
Trademark
Application Date
EMAX
EMAX
97185546 not registered Live/Pending
eMax Holdings, LLC
2021-12-22
EMAX
EMAX
97185517 not registered Live/Pending
eMax Holdings, LLC
2021-12-22
EMAX
EMAX
97105469 not registered Live/Pending
MAXIN SMART MANUFACTURING CO., LTD.
2021-11-02
EMAX
EMAX
90602005 not registered Live/Pending
Sigma Powertrain, Inc.
2021-03-25
EMAX
EMAX
90079008 not registered Live/Pending
Encompass Group, LLC
2020-07-28
EMAX
EMAX
87524764 not registered Dead/Abandoned
303 Management, Inc.
2017-07-12
EMAX
EMAX
86958875 not registered Dead/Abandoned
YINYAN TECH US INC.
2016-03-30
EMAX
EMAX
86935563 5121123 Live/Registered
Mewah Brands (S) Pte Ltd
2016-03-10
EMAX
EMAX
86175593 not registered Dead/Abandoned
Farid, Tariq
2014-01-27
EMAX
EMAX
85967327 not registered Dead/Abandoned
United States Global Trading Services LLC
2013-06-22
EMAX
EMAX
85249892 4028598 Live/Registered
E-ONE, Inc.
2011-02-23
EMAX
EMAX
85246183 4026089 Live/Registered
E-ONE, Inc.
2011-02-18

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