FDA UDI In Commercial Distribution 🇺🇸 United States

LO

DI: 00813110028136 · Model: 260-250-503 · BICON, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LO
Primary DI
00813110028136
Version / Model
260-250-503
Catalog Number
260-250-503
Company Name
BICON, LLC
Labeler DUNS
945015758
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-01
Public Version
3
Public Version Date
2021-10-27
Public Version Status
Update
Public Device Record Key
757005af-dd42-4149-877d-e8d00ace6ada

Device Description

3.0mm Overdenture Abutment - 2.5mm Post

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
No
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
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary 00813110028136

Customer Contacts

Phone
617-524-4443

Premarket Submissions

Submission Number Supplement Number
K853788 000