FDA UDI In Commercial Distribution 🇺🇸 United States

Bonafix

DI: 00850074346159 · Model: BTIM5008N · Zentek Medical LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bonafix
Primary DI
00850074346159
Version / Model
BTIM5008N
Company Name
Zentek Medical LLC
Labeler DUNS
086804993
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-03
Public Version
1
Public Version Date
2025-06-11
Public Version Status
New
Public Device Record Key
c33e0591-967a-42db-a33d-dbba63be3dae

Device Description

Bonafix Two Implant 5.00 x 8mm Finished

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
No
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 00850074346159

Customer Contacts

Phone
7329792502

Premarket Submissions

Submission Number Supplement Number
K213677 000