FDA UDI In Commercial Distribution 🇺🇸 United States

DynaBlast

DI: D7681022010300 · Model: 10.220.1030 · KEYSTONE DENTAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DynaBlast
Primary DI
D7681022010300
Version / Model
10.220.1030
Catalog Number
10.220.1030
Company Name
KEYSTONE DENTAL, INC.
Labeler DUNS
787471015
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-02-04
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
62a8806a-5805-4b8a-a1ce-247f3f2b4f5e

Device Description

Biomaterials

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
NUN BONE GRAFTING MATERIAL, HUMAN SOURCE

GMDN Terms

Code Name
47970 Dental bone matrix implant, human-derived

Identifiers

Type ID
Primary D7681022010300

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K060332 000

Device Sizes

Type Value Unit Text
Device Size Text, specify .5cc - 5cc