FDA UDI In Commercial Distribution 🇺🇸 United States

SuperLine

DI: D755FX5014SWC0 · Model: FX5014SWC · DENTIUM USA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SuperLine
Primary DI
D755FX5014SWC0
Version / Model
FX5014SWC
Catalog Number
FX5014SWC
Company Name
DENTIUM USA
Labeler DUNS
079689366
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-29
Public Version
5
Public Version Date
2025-01-03
Public Version Status
Update
Public Device Record Key
ab222c03-fd4a-47d6-bf33-2faa396581c4

Device Description

Endosseous dental implant

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
MR Conditional
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
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 D755FX5014SWC0

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K160965 000

Device Sizes

Type Value Unit Text
Length 14 Millimeter
Outer Diameter 5 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Stored and transported in a dry condition in the original package at room temperature and kept away from sunlight.