L2/L5 LIGHT GUIDE

GUDID 04719873120550

BONART CO., LTD.

Dental laboratory curing unit
Primary Device ID04719873120550
NIH Device Record Keyda888b59-4c30-4a47-8971-640f7414cea1
Commercial Distribution StatusIn Commercial Distribution
Brand NameL2/L5 LIGHT GUIDE
Version Model NumberLC0007-082
Company DUNS657263687
Company NameBONART CO., 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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104719873120550 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EBZActivator, Ultraviolet, For Polymerization

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-07-31
Device Publish Date2016-09-20

Devices Manufactured by BONART CO., LTD.

04719873121533 - ART TRIPLE BEND 25kHz2023-04-03
04719873121540 - ART TRIPLE BEND 30kHz2023-04-03
04719873121410 - PIEZO TIP/BE-P2022-03-28
04719873121366 - 25K FS-SLIM PLASTIC INSERT/Darby2021-01-04
04719873121373 - 30K FS-SLIM PLASTIC INSERT/Darby2021-01-04
04719873121380 - 25K FS-10 PLASTIC INSERT/Darby2021-01-04
04719873121397 - 30K FS-10 PLASTIC INSERT/Darby2021-01-04
04719873121359 - BONE TIP/BM-PS12020-09-25

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