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Defend

FDA UDI

Class II (US FDA UDI)

by Young Innovations, Inc.

Identity

Trade Name
Defend FDA UDI
Generic Name
Dental prosthesis veneer resin FDA UDI
Device Name
NH Flowable Composite, 2 Syringe Kit 2g x 2, w/Syringe Tips, Shade A3 FDA UDI
Model / Reference
CMP-F303 FDA UDI
Description
NH Flowable Composite, 2 Syringe Kit 2g x 2, w/Syringe Tips, Shade A3 FDA UDI

Identifiers

Primary DI / UDI-DI
00840326421208 FDA UDI
510(k) Number
K121915 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental prosthesis veneer 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 prosthesis veneer resin

Defend by Young Innovations, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental prosthesis veneer resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7bf71df5-b672-40fe-848c-c689f8bacf82 36 fields · synced May 30, 2026