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EdgeTaper™

FDA UDI

Class I (US FDA UDI)

by US Endodontics, LLC

Identity

Trade Name
EdgeTaper™ FDA UDI
Generic Name
Synthetic gutta-percha FDA UDI
Device Name
Slim Fit EdgeTaper Gutta Percha Points F2 FDA UDI
Model / Reference
ETF2GP FDA UDI
Description
Slim Fit EdgeTaper Gutta Percha Points F2 FDA UDI

Identifiers

Catalog Number
ETF2GP FDA UDI
Primary DI / UDI-DI
00818365027989 FDA UDI
FDA Product Code
EKM FDA UDI
GMDN Term
Synthetic gutta-percha FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3850 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Synthetic gutta-percha

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

Similar devices

Also classified as Synthetic gutta-percha.

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 9a281385-4c06-493f-98fe-13bc0e75e84d 35 fields · synced May 30, 2026