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Preat

FDA UDI

Class I (US FDA UDI)

by PREAT Corporation

Identity

Trade Name
Preat FDA UDI
Generic Name
Dental implant system FDA UDI
Device Name
PreatLoc™ Parallel Post 4 Pack FDA UDI
Model / Reference
7100021-4 FDA UDI
Description
PreatLoc™ Parallel Post 4 Pack FDA UDI

Identifiers

Catalog Number
7100021-4 FDA UDI
Primary DI / UDI-DI
00842092186626 FDA UDI
FDA Product Code
EIL FDA UDI
GMDN Term
Dental implant system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant system

Preat by PREAT Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PREAT Corporation

Sources (1)

  • FDA UDI 4dd781a3-1650-4432-a1d9-6b353fd420a4 35 fields · synced May 31, 2026