FDA UDI In Commercial Distribution 🇺🇸 United States

Diamodent

DI: D907R8010 · Model: N/A · DIAMODENT INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Diamodent
Primary DI
D907R8010
Version / Model
N/A
Catalog Number
R801
Company Name
DIAMODENT INC
Labeler DUNS
013827410
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-20
Public Version
1
Public Version Date
2019-01-21
Public Version Status
New
Public Device Record Key
33ad2782-830c-422a-82ff-06185a4f160e

Device Description

Compatible with: 4.5mm Platform Screw-Vent Zimmer implants Temporary Abutment, Titanium Non-Hexed, 1mm Collar, 5.4mm Profile

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Dry Heat Sterilization

Product Codes

Code Name
DZE Implant, Endosseous, Root-Form

GMDN Terms

Code Name
44880 Dental implant suprastructure, temporary, preformed, single-use

Identifiers

Type ID
Primary D907R8010

Premarket Submissions

Submission Number Supplement Number
K010619 000