Two Striper

FDA UDI

Class I (US FDA UDI)

by Abrasive Technology, Llc

Identity

Trade Name: Two Striper FDA UDI
Generic Name: Root canal post, preformed FDA UDI
Device Name: Dental Root Canal Post FDA UDI
Model / Reference: SNOWLIGHT REFILL- 1.4MM 10 PCS FDA UDI
Description: Dental Root Canal Post FDA UDI

Identifiers

Catalog Number: C831003 FDA UDI
Primary DI / UDI-DI: B868C8310031 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Root canal post, preformed

Two Striper by Abrasive Technology, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Flexi-Overdenture — ESSENTIAL DENTAL SYSTEMS, INC. · Class I
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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: Abrasive Technology, Llc

Sources (1)

FDA UDI 79035303-8192-4256-9204-78f21f0e67f6 34 fields · synced May 30, 2026