FDA UDI In Commercial Distribution 🇺🇸 United States

Stage 1

DI: D76842001K · Model: 42001K · KEYSTONE DENTAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Stage 1
Primary DI
D76842001K
Version / Model
42001K
Catalog Number
42001K
Company Name
KEYSTONE DENTAL, INC.
Labeler DUNS
787471015
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-11
Public Version
5
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
398fc867-7304-4f82-875d-40599b6b3263

Device Description

Angled Abutment

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
NHA ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary D76842001K

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K032495 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Outer Diameter 2.1 - 7.1mm