ACCESSORY ESSENTIALS

GUDID 00031568323775

FGX INTERNATIONAL INC.

Prescription spectacles Prescription spectacles Prescription spectacles Prescription spectacles Prescription spectacles Prescription spectacles Prescription spectacles Prescription spectacles Prescription spectacles Prescription spectacles Prescription spectacles Prescription spectacles Prescription spectacles Prescription spectacles Prescription spectacles
Primary Device ID00031568323775
NIH Device Record Key82b5f963-51a6-4143-91dc-356a88b377fd
Commercial Distribution StatusIn Commercial Distribution
Brand NameACCESSORY ESSENTIALS
Version Model Number10402921.CGU
Company DUNS062312087
Company NameFGX INTERNATIONAL INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
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

Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com
Phone+1(401)231-3800
EmailCustomerservices@fgxi.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100031568323775 [Primary]

FDA Product Code

HOISpectacle, magnifying

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-19
Device Publish Date2022-10-11

On-Brand Devices [ACCESSORY ESSENTIALS]

0003156863330010401050.CTS
0003156863329410401049.CTS
0003156863328710401048.CTS
0003156863327010401047.CTS
0003156819790110400697.CTS
0003156819788810400695.CTS
0003156819592110400694.CTS
0003156819583910400693.CTS
0088766196881410401658.CGU
0088766178005810401342.CTS
0088766167442510401274.ARM
0088766136845410402168.FWG
0088766136837910402166.FWG
0088766136835510402165.FWG
0088766132175610402043.FGX
0088766132172510402073.FGX
0088766130371410402054.RSF
0088766130366010402057.RSF
0088766127672810402047.FMY
0088766127666710402049.FMY
0088766126822810402043.RSF
0088766126821110402041.RSF
0088766126819810402042.RSF
0088766126818110402040.RSF
0088766126817410402039.RSF
0088766126813610402038.RSF
0088766126808210402037.RSF
0088766126803710402036.RSF
0088766111052710401893.FDG
0088766107963310401891.SDM
0088766101987510401721.CTS
0019303340447810402772.KGR
0019303339707710402724.CGU
0019303339693310402722.CGU
0019303339692610402721.CGU
0019303338794810402739.MCV
0019303338793110402737.MCV
0019303338792410402734.MCV
0019303338791710402735.MCV
0019303338790010402738.MCV
0019303338789410402736.MCV
0019303338788710402744.MCV
0019303338787010402743.MCV
0019303338786310402742.MCV
0019303338785610402740.MCV
0019303338784910402741.MCV
0019303338014710402723.CGU
0019303338009310402751.CGU
0019303338008610402750.CGU
0019303338002410402752.CGU

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