FDA UDI In Commercial Distribution 🇺🇸 United States

DIO PROTEM IMPLANT SYSTEM

DI: 08800049214749 · Model: MFP 25410 · DIO Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DIO PROTEM IMPLANT SYSTEM
Primary DI
08800049214749
Version / Model
MFP 25410
Catalog Number
MFP 25410
Company Name
DIO Corporation
Labeler DUNS
631085206
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-01
Public Version
1
Public Version Date
2022-03-09
Public Version Status
New
Public Device Record Key
133be30e-dd76-4c0c-a52a-4498811c926c

Device Description

DIO Protein Implant System consists of Protein Implants, Superstructure, Prosthetics and Surgical Instruments. The Protein Implants is an integrated system of endosseous dental implants which designed to protect main implant from immediate loading during osteointegration period, to increase indurance of temporary tooth and to conduct the immediate functions and immediate recovery of aesthetics of osteoimplanted area. These are made of titanium alloy which have a sandblasted, RBM(Resorbable Blast Media) treated surface. These implants are consist of one-stage, root-form dental implants which provide the clinician to maintain the patients' gingival contour. The Implants have the diameter(2.0/2.5mm) and length.(8/10/12/14mm). The superstructures consist of Protein Cemented Abutment, Ball Cap and Healing Cap. The Protein Cemented Abutments are made of titanium and intended for cement-retained restorations where conventional crown & bridge techniques are required. It can be used for single or multiple unit restorations. Ball Cap intended to retain the O-ring inside of the denture. Healing Cap is fixed on the ball type fixture to protect the direct pressure reduce the motion of fixture. The Prosthetics and Surgical Instruments provide the clinician to choose only those components required for each clinical situation. The implants are gamma sterilized and intended to single use. And the surgical tools are nongamma sterilized and have to be sterilized by user before using.

Device Characteristics

Single Use
Yes
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
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DZE Implant, Endosseous, Root-Form

GMDN Terms

Code Name
55849 Screw endosteal dental implant, two-piece

Identifiers

Type ID
Primary 08800049214749

Customer Contacts

Phone
213-365-2875

Premarket Submissions

Submission Number Supplement Number
K080126 000

Device Sizes

Type Value Unit Text
Device Size Text, specify ® Ø2.5X10mm

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
1 – 30 Degrees Celsius