FDA UDI In Commercial Distribution 🇺🇸 United States

Glidewell IH™

DI: D745701073PRA01150 · Model: 70-1073-PRA0115 · Prismatik Dentalcraft, Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Glidewell IH™
Primary DI
D745701073PRA01150
Version / Model
70-1073-PRA0115
Catalog Number
70-1073-PRA0115
Company Name
Prismatik Dentalcraft, Inc
Labeler DUNS
022761689
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-19
Public Version
1
Public Version Date
2025-06-27
Public Version Status
New
Public Device Record Key
9a9e495f-514b-4380-a003-cbffa113843a

Device Description

Glidewell IH™ Implant Titanium Abutment 3.0 mmP x 6 mmH

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
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
NHA Abutment, implant, dental, endosseous

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary D745701073PRA01150

Premarket Submissions

Submission Number Supplement Number
K153099 000