UF(II) Fixture UF(II) 5005S

GUDID 08806195983607

DIO Corporation

Screw endosteal dental implant, two-piece
Primary Device ID08806195983607
NIH Device Record Key99587729-e001-4e3f-bc07-a642b0dc6711
Commercial Distribution StatusIn Commercial Distribution
Brand NameUF(II) Fixture
Version Model NumberUF(II) 5005S
Catalog NumberUF(II) 5005S
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108806195983607 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DZEImplant, Endosseous, Root-Form

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-04-07
Device Publish Date2022-03-30

On-Brand Devices [UF(II) Fixture]

08806195983799UF(II) 6505UV3
08806195983782UF(II) 6005UV3
08806195983775UF(II) 5505UV3
08806195983768UF(II) 5005UV3
08806195983751UF(II) 4505UV3
08806195983744UF(II) 4007UV3
08806195983737UF(II) 4005UV3
08806195983720UF(II) 7005SF
08806195983713UF(II) 6505SF
08806195983706UF(II) 6005SF
08806195983690UF(II) 5505SF
08806195983683UF(II) 5005SF
08806195983676UF(II) 4505SF
08806195983669UF(II) 4007SF
08806195983652UF(II) 4005SF
08806195983645UF(II) 7005S
08806195983638UF(II) 6505S
08806195983621UF(II) 6005S
08806195983614UF(II) 5505S
08806195983607UF(II) 5005S
08806195983591UF(II) 4505S
08806195983584UF(II) 4007S
08806195983577UF(II) 4005S

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