FDA.reportPublic FDA data

Healing Abutment

Primary DI
08806388287819
Brand
Healing Abutment
Company
Megagen Implant Co. Ltd
Model
AOHS50655
Catalog number
AOHS50655T
Device description
AnyOne Internal & ST Implant System (S2) S/ M5/ L6.5/ H=5/ Hex
Published
2023-06-08
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
OTC
false
Sterile
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
K210826000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K210826000Healing Abutment, Cover ScrewMegagen Implant Co., Ltd.2022-02-03NHA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08806388287819PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08806388287819088063882878198806388287819

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.

Regulatory Flags#

DUNS number
687388178
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
true
Manufacturing date on label
true
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
08806388287857Healing AbutmentAOHS50704AOHS50704T2023-06-30
08806388287826Healing AbutmentAOHS50657AOHS50657T2023-06-08
08806388287833Healing AbutmentAOHS50702AOHS50702T2023-06-08
08806388287840Healing AbutmentAOHS50703AOHS50703T2023-06-08
08806388287864Healing AbutmentAOHS50705AOHS50705T2023-06-08
08806388287871Healing AbutmentAOHS50707AOHS50707T2023-06-08
08806388287888Healing AbutmentAOHS60702AOHS60702T2023-06-08
08806388287895Healing AbutmentAOHS60703AOHS60703T2023-06-08
08806388287901Healing AbutmentAOHS60704AOHS60704T2023-06-08
08806388287918Healing AbutmentAOHS60705AOHS60705T2023-06-08
08806388287925Healing AbutmentAOHS60707AOHS60707T2023-06-08
08806388287932Healing AbutmentAOHS60802AOHS60802T2023-06-08
08806388287949Healing AbutmentAOHS60803AOHS60803T2023-06-08
08806388288359Healing AbutmentAOHS50654NAOHS50654NT2023-06-08
08806388288366Healing AbutmentAOHS50655NAOHS50655NT2023-06-08
08806388288373Healing AbutmentAOHS50657NAOHS50657NT2023-06-08
08806388288380Healing AbutmentAOHS50702NAOHS50702NT2023-06-08
08806388288397Healing AbutmentAOHS50703NAOHS50703NT2023-06-08
08806388288403Healing AbutmentAOHS50704NAOHS50704NT2023-06-08
08806388288410Healing AbutmentAOHS50705NAOHS50705NT2023-06-08

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Primary DI, Brand, Company table
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