UV Active Implant System UF(II) 6511UV3

GUDID 08800049232248

DIO Corporation

Screw endosteal dental implant, two-piece
Primary Device ID08800049232248
NIH Device Record Keyd9b69d05-21e5-4a75-b91c-de417ae30561
Commercial Distribution StatusIn Commercial Distribution
Brand NameUV Active Implant System
Version Model NumberUF(II) 6511UV3
Catalog NumberUF(II) 6511UV3
Company DUNS631085206
Company NameDIO Corporation
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 Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800049232248 [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 Date2020-01-20
Device Publish Date2020-01-10

On-Brand Devices [UV Active Implant System]

08800049232330UF(II)N 3313UV3
08800049232323UF(II)N 3311UV3
08800049232316UF(II)N 3310UV3
08800049232309UF(II)N 3308UV3
08800049232293UF(II)N 3013UV3
08800049232286UF(II)N 3011UV3
08800049232279UF(II)N 3010UV3
08800049232262UF(II)N 3008UV3
08800049231982UF(II) 4010UV3
08800049231975UF(II) 4008UV3
08800049231968UF(II) 3813UV3
08800049231951UF(II) 3811UV3
08800049231944UF(II) 3810UV3
08800049231937UF(II) 3808UV3
08800049232255UF(II) 6513UV3
08800049232248UF(II) 6511UV3
08800049232231UF(II) 6510UV3
08800049232224UF(II) 6508UV3
08800049232217UF(II) 6507UV3
08800049232200UF(II) 6013UV3
08800049232194UF(II) 6011UV3
08800049232187UF(II) 6010UV3
08800049232170UF(II) 6008UV3
08800049232163UF(II) 6007UV3
08800049232156UF(II) 5513UV3
08800049232149UF(II) 5511UV3
08800049232132UF(II) 5510UV3
08800049232125UF(II) 5508UV3
08800049232118UF(II) 5507UV3
08800049232101UF(II) 5013UV3
08800049232095UF(II) 5011UV3
08800049232088UF(II) 5010UV3
08800049232071UF(II) 5008UV3
08800049232064UF(II) 5007UV3
08800049232057UF(II) 4513UV3
08800049232040UF(II) 4511UV3
08800049232033UF(II) 4510UV3
08800049232026UF(II) 4508UV3
08800049232019UF(II) 4507UV3
08800049232002UF(II) 4013UV3
08800049231999UF(II) 4011UV3
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.