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Edge Apex™

FDA UDI

Class I (US FDA UDI)

by US Endodontics, LLC

Identity

Trade Name
Edge Apex™ FDA UDI
Generic Name
Endodontic apex locator FDA UDI
Device Name
Edge Apex Tester FDA UDI
Model / Reference
EEALUT FDA UDI
Description
Edge Apex Tester FDA UDI

Identifiers

Catalog Number
EEALUT FDA UDI
Primary DI / UDI-DI
00818365028962 FDA UDI
510(k) Number
K181087 FDA UDI
FDA Product Code
EKX FDA UDI
GMDN Term
Endodontic apex locator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endodontic apex locator

Edge Apex™ by US Endodontics, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic apex locator.

Cleared under the same submission

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 1165fdf5-fa9c-43d8-acf3-eac17c7c6bac 36 fields · synced May 30, 2026