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3D Endo

FDA UDI

Class I (US FDA UDI)

by 3d Dental Designs And Development, Llc

Identity

Trade Name
3D Endo FDA UDI
Generic Name
Manual endodontic file/rasp, single-use FDA UDI
Device Name
K-File NiTi 25mm #60 6/Pk FDA UDI
Model / Reference
KN2560 FDA UDI
Description
K-File NiTi 25mm #60 6/Pk FDA UDI

Identifiers

Catalog Number
KN2560 FDA UDI
Primary DI / UDI-DI
00810126501844 FDA UDI
FDA Product Code
EKS FDA UDI
GMDN Term
Manual endodontic file/rasp, single-use 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual endodontic file/rasp, single-use

3D Endo by 3d Dental Designs And Development, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual endodontic file/rasp, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI beca15d6-ad55-471e-9db7-eca494914a69 35 fields · synced May 31, 2026