FDA UDI In Commercial Distribution 🇺🇸 United States

Preat

DI: 00842092185995 · Model: 7100004-20 · Preat Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Preat
Primary DI
00842092185995
Version / Model
7100004-20
Catalog Number
7100004-20
Company Name
Preat Corporation
Labeler DUNS
117776048
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-22
Public Version
1
Public Version Date
2025-12-30
Public Version Status
New
Public Device Record Key
e26a29d6-b09b-48a0-b3c6-dec354c1d1d3

Device Description

PreatLoc™ Clear Replacement Insert 20 Pack

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
MR Conditional
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 00842092185995

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K251547 000