← Back to catalogue

VersaFlo

FDA UDI

Class II (US FDA UDI)

by Centrix, Inc.

Identity

Trade Name
VersaFlo FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
VersaFlo A1 prefilled NeedleTube, 16 pk FDA UDI
Model / Reference
330501 FDA UDI
Description
VersaFlo A1 prefilled NeedleTube, 16 pk FDA UDI

Identifiers

Primary DI / UDI-DI
00817051020839 FDA UDI
510(k) Number
K960667 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

Yes

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

VersaFlo by Centrix, Inc. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Centrix, Inc.

Sources (1)

  • FDA UDI 0f5824a1-94dd-4eb2-9923-aea0cb33f351 34 fields · synced Jun 7, 2026