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RE-GEN Flowable Composite Shade A2

FDA UDI

Class II (US FDA UDI)

by Vista Dental

Identity

Trade Name
RE-GEN Flowable Composite Shade A2 FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
RE-GEN Flowable Composite Shade A2 FDA UDI
Model / Reference
1 FDA UDI
Description
RE-GEN Flowable Composite Shade A2 FDA UDI

Identifiers

Catalog Number
90648 FDA UDI
Primary DI / UDI-DI
00850194007756 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
Not 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

RE-GEN Flowable Composite Shade A2 by Vista Dental — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 94d9aef6-6cf4-462c-835a-eefe28354818 36 fields · synced May 30, 2026