SOLUUT PX ANTERIOR

GUDID 04582276053356

YAMAHACHI DENTAL MFG.,CO.

Resin artificial teeth
Primary Device ID04582276053356
NIH Device Record Keyfb30c7e1-4a38-4cb0-9810-9a45f23a537d
Commercial Distribution StatusIn Commercial Distribution
Brand NameSOLUUT PX ANTERIOR
Version Model NumberC7, W0.5
Company DUNS693430001
Company NameYAMAHACHI DENTAL MFG.,CO.
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104582276053356 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ELMDenture, Plastic, Teeth

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-10-25
Device Publish Date2021-10-16

On-Brand Devices [SOLUUT PX ANTERIOR]

04582276058405T7, A1
04582276058221T6, A1
04582276058047T5, A1
04582276057866T4, A1
04582276057651SS7, A1
04582276057477SS6, A1
04582276057293SS5, A1
04582276057118SS4, A1
04582276056906S7, A1
04582276056722S6, A1
04582276056548S5, A1
04582276056364S4, A1
04582276055046LS5, A1
04582276054919LS4, B1
04582276054704L7, B1
04582276054155L4, A4
04582276053004C6, A1
04582276052847C5, A3
04582276052823C5, A1
04582276055213LS5, W0.5
04582276053356C7, W0.5

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