Versatile Implant Pack

Primary DI
D824PVRH60082
Brand
Versatile Implant Pack
Company
SURGIKOR, LLC
Model
PVRH6008
Device description
Ø6.0mm x L8.0mm, Hex Connection, Regular Platform with Cover Screw & Mount
Published
2017-02-07
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
DZEImplant, Endosseous, Root-Form

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DZEImplant, Endosseous, Root-FormDental2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K152555000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K152555000Dental Implant SystemAriabio International, Inc.2016-02-11DZE

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
D824PVRH60081PackageHIBCC10In Commercial Distribution
D824PVRH60082PackageHIBCC4In Commercial Distribution
D824PVRH60080PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Basket endosteal dental implant, two-pieceA sterile device made of alloplastic materials [e.g., titanium (Ti), stainless steel, ceramic] intended to be surgically implanted into alveolar and/or basal bone of the mandible or maxilla to provide support and a means of retention for a dental prosthesis (e.g., bridge, single-tooth, overdenture). It is a two-piece device composed of an anchorage component (implant body) in the form of a single, double, and/or triple contiguous cylinder(s) that is implanted into bone, and a retention component (implant abutment), typically attached to the anchorage component after implantation, that protrudes through gingival tissues to support the prosthesis.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
080321629
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
true
Combination product
false
Lot or batch
true
Serial number
true
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
D824FRC43100Fixation OneFRC43102025-12-15
D824FRC43110Fixation OneFRC43112025-12-15
D824FRC43130Fixation OneFRC43132025-12-15
D824FRC43150Fixation OneFRC43152025-12-15
D824FRC43180Fixation OneFRC43182025-12-15
D824FRC50080Fixation OneFRC50082025-12-15
D824FRC50100Fixation OneFRC50102025-12-15
D824FRC50110Fixation OneFRC50112025-12-15
D824FRC50130Fixation OneFRC50132025-12-15
D824FRC50150Fixation OneFRC50152025-12-15
D824FRC50180Fixation OneFRC50182025-12-15
D824MU17RC20Multi-Unit AbutmentMU17RC22025-12-15
D824MU17RC30Multi-Unit AbutmentMU17RC32025-12-15
D824MU17WC20Multi-Unit AbutmentMU17WC22025-12-15
D824MU17WC30Multi-Unit AbutmentMU17WC32025-12-15
D824IRH45070Immediate Implant IRH45072024-09-16
D824PFNC30100Fixation Implant PackPFNC30102017-01-31
D824PFNC30110Fixation Implant PackPFNC30112017-01-31
D824PFNC30130Fixation Implant PackPFNC30132017-01-31
D824PFNC30150Fixation Implant PackPFNC30152017-01-31

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Primary DI, Brand, Company table
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