FineEtch 101-1201

GUDID 08809262954036

37% Phosphoric Acid with semi-gel consistency for controlled contact.

Spident Co., Ltd.

Dental etching solution
Primary Device ID08809262954036
NIH Device Record Key7e991e25-4ea3-45a7-89c2-e539bb77777a
Commercial Distribution StatusIn Commercial Distribution
Brand NameFineEtch
Version Model Number101-1201
Catalog Number101-1201
Company DUNS689370711
Company NameSpident Co., Ltd.
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 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

Customer Support Contacts

Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100194202309204 [Package]
Package: [180 Units]
Discontinued: 2023-09-20
In Commercial Distribution
GS100202202110178 [Package]
Package: [200 Units]
In Commercial Distribution
GS108809262954036 [Primary]
GS120200101161714 [Package]
Package: [100 Units]
Discontinued: 2019-05-16
Not in Commercial Distribution

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-05-17
Device Publish Date2017-02-20

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