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Flows-Rite

FDA UDI

Class II (US FDA UDI)

by Pulpdent Corporation

Identity

Trade Name
FLOWS-RITE FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Refill Kit: 4 x 1.5 gm syringes all one shade + 20 applicator tips Multi-purpose flowable composite and veneer cement FDA UDI
Model / Reference
FK FDA UDI
Description
Refill Kit: 4 x 1.5 gm syringes all one shade + 20 applicator tips Multi-purpose flowable composite and veneer cement FDA UDI

Identifiers

Primary DI / UDI-DI
D701FK2 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

Yes

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

Flows-Rite by Pulpdent Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 666d5c2b-8402-4212-a931-0469f9a215d9 33 fields · synced Jun 9, 2026