FDA UDI In Commercial Distribution 🇺🇸 United States

ACE Surgical

DI: D74520745600 · Model: 2074560 · Prismatik Dentalcraft, Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
ACE Surgical
Primary DI
D74520745600
Version / Model
2074560
Catalog Number
2074560
Company Name
Prismatik Dentalcraft, Inc
Labeler DUNS
022761689
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
5
Public Version Date
2023-08-22
Public Version Status
Update
Public Device Record Key
c009185a-279a-414d-b3a6-78f27a9e4bf7

Device Description

ACE Surgical INTERNAL HEX Titanium Base Abutment, 4.5 Platform, 6 mm

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
DZE IMPLANT, ENDOSSEOUS, ROOT-FORM

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary D74520745600

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Post Height, 6mm