FDA.reportPublic FDA data

I-FIX Angled Type Fixture Healing Abutment

Primary DI
08806169128393
Brand
I-FIX Angled Type Fixture Healing Abutment
Company
DENTIS CO. ,LTD
Model
DMAHA4032NS
Device description
I-FIX Angled Type Fixture Healing Abutment / DMAHA4032NS
Published
2023-05-08
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
NHAAbutment, Implant, Dental, Endosseous

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NHAAbutment, Implant, Dental, EndosseousDental2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K230203000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K230203000Dentis I-FIX AbutmentDentis Co., Ltd.2023-05-03NHA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08806169128393PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08806169128393088061691283938806169128393

GMDN Terms#

Term, Definition table
TermDefinition
Dental implant suprastructure, temporary, preformed, single-useA prefabricated device intended to be used during dental implant restorative and laboratory procedures to provide a temporary intermediate fixture level between a dental implant and a temporary dental prosthesis/restoration, during the oral soft-tissue healing and sculpturing period, prior to the fabrication/rehabilitation and installation of the final prosthesis/restoration (e.g., bridge, single tooth, overdenture). It typically includes burnout/temporary cylinders, fixture impression pick-ups, replica devices, caps/cover screws in a variety of shapes, sizes, and materials [e.g., titanium (Ti), plastic]. This is a single-use device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
694721181
Device count
1
Lot or batch
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
08800313236132SQ AXEL Step DrillDSASTD54122026-05-08
08800053007115i-Clean Solid Abutment DriverDSADS2026-04-22
08800053007122i-Clean Solid Abutment DriverDSADL2026-04-22
08800053023757Bone ProfilerDBP452026-04-22
08800053023764Bone ProfilerDBP552026-04-22
08800053023771Bone ProfilerDBP652026-04-22
08800053032322Bone Profiler BaseDBPBN2026-04-22
08800053032339Bone Profiler BaseDBPBM2026-04-22
08800053032346Bone Profiler BaseDBPBR2026-04-22
08800053034340Surgical SQ KITDSQKN-12026-04-22
08800053038737I-FIX Angled Mount Adapter BodyDNAMB2026-04-22
08800053038744I-FIX Angled Mount Adapter ScrewDNAMS2026-04-22
08800053038751I-FIX Angled Mount AdapterDNAMA2026-04-22
08800053042505I-FIX Bone ProfilerDBPI402026-04-22
08800053043526SQ Guide Profiler DrillDSQGPDM2026-04-22
08800053081030Depth GaugeDSSDGN2026-04-22
08800053081047Bone PackerDSSBPN2026-04-22
08800053081054SAVE 03DSSS03N2026-04-22
08800053083041ReamerDSSR28N2026-04-22
08800053083058ReamerDSSR31N2026-04-22

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Primary DI, Brand, Company table
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