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Flexi-Flow Auto

FDA UDI

Class II (US FDA UDI)

by Essential Dental Systems, Inc.

Identity

Trade Name
Flexi-Flow Auto FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Post Cement Syringeable Chemical Cure Shade A2 FDA UDI
Model / Reference
880-00 FDA UDI
Description
Post Cement Syringeable Chemical Cure Shade A2 FDA UDI

Identifiers

Catalog Number
880-00 FDA UDI
Primary DI / UDI-DI
00766054000082 FDA UDI
510(k) Number
K922249 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 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

Yes

FDA UDI

Category: Dental composite resin

Flexi-Flow Auto by Essential Dental Systems, Inc. — 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 d5756deb-3a58-4bf7-ad1c-7055f3481b22 38 fields · synced May 31, 2026