SilverSense

GUDID 00817051023632

SilverSense Standard Kit

CENTRIX, INC.

Dental coating, tooth-desensitizing, professional
Primary Device ID00817051023632
NIH Device Record Key68bc2748-8a34-4d3f-b30f-246e202b6c67
Commercial Distribution StatusIn Commercial Distribution
Brand NameSilverSense
Version Model Number310172
Company DUNS053707303
Company NameCENTRIX, 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 Usetrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100817051023632 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

PHRDiammine Silver Fluoride Dental Hypersensitivity Varnish

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-12-21
Device Publish Date2023-12-13

On-Brand Devices [SilverSense]

00817051023632SilverSense Standard Kit
00817051023625SilverSense Clinic Kit

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