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RE-GEN Flowable Composite Shade A1

FDA UDI

Class II (US FDA UDI)

by Vista Dental

Identity

Trade Name
RE-GEN Flowable Composite Shade A1 FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
RE-GEN Flowable Composite Shade A1 FDA UDI
Model / Reference
1 FDA UDI
Description
RE-GEN Flowable Composite Shade A1 FDA UDI

Identifiers

Catalog Number
90639 FDA UDI
Primary DI / UDI-DI
00850194007091 FDA UDI
510(k) Number
K062157 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

RE-GEN Flowable Composite Shade A1 by Vista Dental — 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
Vista Dental

Sources (1)

  • FDA UDI f99e7c14-2fe2-4906-897d-cb6c90fc60ec 35 fields · synced May 30, 2026