Flexi-Post Fiber

FDA UDI

Class I (US FDA UDI)

by Essential Dental Systems, Inc.

Identity

Trade Name: Flexi-Post Fiber FDA UDI
Generic Name: Root canal post, preformed FDA UDI
Device Name: Flexi-Post Fiber Refill Kit Size 0 FDA UDI
Model / Reference: 2130-0 FDA UDI
Description: Flexi-Post Fiber Refill Kit Size 0 FDA UDI

Identifiers

Catalog Number: 2130-0 FDA UDI
Primary DI / UDI-DI: 00766054001362 FDA UDI
FDA Product Code: ELR FDA UDI
GMDN Term: Root canal post, preformed FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3810 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Root canal post, preformed

Flexi-Post Fiber by Essential Dental Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Root canal post, preformed.

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Essential Dental Systems, Inc.

Sources (1)

FDA UDI d3b5793a-43dd-49fc-a638-908a02ccb708 35 fields · synced May 31, 2026