← Back to catalogue

GoldenDent

FDA UDI

Class I (US FDA UDI)

by GoldenDent

Identity

Trade Name
GoldenDent FDA UDI
Generic Name
Rotary/reciprocating endodontic file/rasp, reusable FDA UDI
Device Name
Golden-Taper Rotary Pack - Type S2 (6 files) - Length 21mm FDA UDI
Model / Reference
GTS2-21 FDA UDI
Description
Golden-Taper Rotary Pack - Type S2 (6 files) - Length 21mm FDA UDI

Identifiers

Catalog Number
GTS2-21 FDA UDI
Primary DI / UDI-DI
00850028211168 FDA UDI
FDA Product Code
EKS FDA UDI
GMDN Term
Rotary/reciprocating 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: Rotary/reciprocating endodontic file/rasp, reusable

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

Similar devices

Also classified as Rotary/reciprocating endodontic file/rasp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
GoldenDent

Sources (1)

  • FDA UDI ed2b9e78-50ee-48f5-896f-c478220216e0 34 fields · synced May 30, 2026