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EdgeEndo®

FDA UDI

Class U (US FDA UDI)

by US Endodontics, LLC

Identity

Trade Name
EdgeEndo® FDA UDI
Generic Name
Dental root surface conditioner FDA UDI
Device Name
EdgeIce™ 0 FDA UDI
Model / Reference
100818365020058 FDA UDI
Description
EdgeIce™ 0 FDA UDI

Identifiers

Catalog Number
100818365020058 FDA UDI
Primary DI / UDI-DI
00818365029006 FDA UDI
FDA Product Code
KJJ FDA UDI
GMDN Term
Dental root surface conditioner FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental root surface conditioner

EdgeEndo® by US Endodontics, LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental root surface conditioner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
US Endodontics, LLC

Sources (1)

  • FDA UDI 7aa9fbc5-c204-48d0-b27d-ffb14ece9302 35 fields · synced May 30, 2026