BIOLIGHT DRILL FREE

GUDID 10667147000453

BIOLIGHT DRILL FREE # 4

Synca Marketing Inc

Root canal post, preformed
Primary Device ID10667147000453
NIH Device Record Key03f4052b-a8ed-4c8a-8b93-8b5a47a64f1e
Commercial Distribution Discontinuation2023-02-13
Commercial Distribution StatusNot in Commercial Distribution
Brand NameBIOLIGHT DRILL FREE
Version Model NumberBDF04
Company DUNS247111768
Company NameSynca Marketing Inc
Device Count10
DM Exemptfalse
Pre-market Exempttrue
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110667147000453 [Primary]
GS110667147100450 [Unit of Use]

FDA Product Code

ERLDrill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2025-07-08
Device Publish Date2023-02-13

On-Brand Devices [BIOLIGHT DRILL FREE]

10667147000491BIOLIGHT DRILL FREE KIT
10667147100481BIOLIGHT DRILL FREE #12
10667147100474BIOLIGHT DRILL FREE #9
10667147100467BIOLIGHT DRILL FREE #6
10667147000453BIOLIGHT DRILL FREE # 4

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.