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GoldenDent

FDA UDI

Class I (US FDA UDI)

by GoldenDent

Identity

Trade Name
GoldenDent FDA UDI
Generic Name
Manual endodontic file/rasp, reusable FDA UDI
Device Name
Golden K File SS-Size #40 25mm Length FDA UDI
Model / Reference
GK40 FDA UDI
Description
Golden K File SS-Size #40 25mm Length FDA UDI

Identifiers

Catalog Number
GK40 FDA UDI
Primary DI / UDI-DI
00850011211489 FDA UDI
FDA Product Code
EKS FDA UDI
GMDN Term
Manual endodontic file/rasp, reusable 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Manual endodontic file/rasp, reusable

GoldenDent by GoldenDent — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual endodontic file/rasp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
GoldenDent

Sources (1)

  • FDA UDI 86e32b20-8bbc-4ceb-8fbf-4b02ba8474d7 34 fields · synced May 30, 2026