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Beautifil Flow Plus X

FDA UDI

Class II (US FDA UDI)

by Shofu Dental Corp.

Identity

Trade Name
BEAUTIFIL FLOW PLUS X FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
BEAUTIFIL PLUS X TIP F00B2 FDA UDI
Model / Reference
Y2407 FDA UDI
Description
BEAUTIFIL PLUS X TIP F00B2 FDA UDI

Identifiers

Catalog Number
Y2407 FDA UDI
Primary DI / UDI-DI
E235Y24070 FDA UDI
510(k) Number
K172530 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental composite resin

Beautifil Flow Plus X by Shofu Dental Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shofu Dental Corp.

Sources (1)

  • FDA UDI 24794c15-5d58-4d58-b19a-6e6730d3be9b 36 fields · synced Jun 8, 2026