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Beautifil Flow Plus

FDA UDI

Class II (US FDA UDI)

by Shofu Dental Corp.

Identity

Trade Name
Beautifil Flow Plus FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
BFP F00 / Beautibond FDA UDI
Model / Reference
2002B FDA UDI
Description
BFP F00 / Beautibond FDA UDI

Identifiers

Catalog Number
2002B FDA UDI
Primary DI / UDI-DI
E2352002B0 FDA UDI
510(k) Number
K101603 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 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 59790ee9-091e-4b26-a06a-fb0170e23922 37 fields · synced May 30, 2026