FDA UDI In Commercial Distribution 🇺🇸 United States

OptraSculpt

DI: 07615208296754 · Model: 639792AN · IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
60

Basic Information

Brand Name
OptraSculpt
Primary DI
07615208296754
Version / Model
639792AN
Catalog Number
639792AN
Company Name
IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Labeler DUNS
448015938
Distribution Status
In Commercial Distribution
Device Count in Pkg
60
Record Status
Published
Publish Date
2026-01-15
Public Version
1
Public Version Date
2026-01-23
Public Version Status
New
Public Device Record Key
f02cc6be-1928-49fa-8eba-83563595c5c9

Device Description

OptraSculpt Pad Refill/4 mm/60

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KXR APPLICATOR, RESIN

GMDN Terms

Code Name
41861 Dental restoration carver, resin

Identifiers

Type ID
Package 07615208445947
Primary 07615208296754
Unit of Use 07615208472516
Previous DVIV639792AN1