Plastic Cylinder

GUDID 08800049241820

DIO Corporation

Dental implant suprastructure, temporary, preformed, single-use
Primary Device ID08800049241820
NIH Device Record Keyf6639e54-b545-48f5-8081-48ec0dd96969
Commercial Distribution StatusIn Commercial Distribution
Brand NamePlastic Cylinder
Version Model NumberAPI 48514N[H]
Company DUNS631085206
Company NameDIO Corporation
Device Count1
DM Exempttrue
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 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
GS108800049241820 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DZEImplant, Endosseous, Root-Form

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800049241820]

Moist Heat or Steam Sterilization


[08800049241820]

Moist Heat or Steam Sterilization


[08800049241820]

Moist Heat or Steam Sterilization


[08800049241820]

Moist Heat or Steam Sterilization


[08800049241820]

Moist Heat or Steam Sterilization


[08800049241820]

Moist Heat or Steam Sterilization


[08800049241820]

Moist Heat or Steam Sterilization


[08800049241820]

Moist Heat or Steam Sterilization


[08800049241820]

Moist Heat or Steam Sterilization


[08800049241820]

Moist Heat or Steam Sterilization


[08800049241820]

Moist Heat or Steam Sterilization


[08800049241820]

Moist Heat or Steam Sterilization


[08800049241820]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-09-23
Device Publish Date2025-09-15

On-Brand Devices [Plastic Cylinder ]

08800049241820API 48514N[H]
08800049241806API 48514[H]

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