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Venus Pearl

FDA UDI

Class II (US FDA UDI)

by Kulzer, Inc.

Identity

Trade Name
Venus Pearl FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Venus Pearl PLT Refill 10x0,2G ODC FDA UDI
Model / Reference
66048093 FDA UDI
Description
Venus Pearl PLT Refill 10x0,2G ODC FDA UDI

Identifiers

Catalog Number
66048093 FDA UDI
Primary DI / UDI-DI
J014660480930 FDA UDI
510(k) Number
K112501 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental composite resin

Venus Pearl by Kulzer, 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

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Manufacturer

Manufacturer
Kulzer, Inc.

Sources (1)

  • FDA UDI 66dcdbf5-e5d3-4f31-bd99-cf561903fe0c 36 fields · synced May 30, 2026