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EdgeVerify

FDA UDI

Class I (US FDA UDI)

by US Endodontics, LLC

Identity

Trade Name
EdgeVerify FDA UDI
Generic Name
Warm-bonded endodontic obturation system obturator FDA UDI
Device Name
Endodontic Verifier FDA UDI
Model / Reference
X74506V FDA UDI
Description
Endodontic Verifier FDA UDI

Identifiers

Catalog Number
X74506V FDA UDI
Primary DI / UDI-DI
00819514024224 FDA UDI
FDA Product Code
EIL FDA UDI
GMDN Term
Warm-bonded endodontic obturation system obturator 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Warm-bonded endodontic obturation system obturator

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

Similar devices

Also classified as Warm-bonded endodontic obturation system obturator.

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 b3017168-24f5-43ad-947e-bc02ef588068 35 fields · synced Jun 8, 2026