FDA UDI Not in Commercial Distribution 🇺🇸 United States

Overdenture Titanium Coping

DI: 10841307109136 · Model: 1000-65 · IMPLANT DIRECT SYBRON MANUFACTURING LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Overdenture Titanium Coping
Primary DI
10841307109136
Version / Model
1000-65
Catalog Number
1000-65
Company Name
IMPLANT DIRECT SYBRON MANUFACTURING LLC
Labeler DUNS
868856969
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
7
Public Version Date
2021-12-31
Public Version Status
Update
Public Device Record Key
27dd0818-5e82-4f76-ac5c-34aa22889d45
Distribution End Date
2021-12-31

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Moist Heat or Steam Sterilization

Product Codes

Code Name
NHA Abutment, Implant, Dental, Endosseous

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary 10841307109136

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K060063 000