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DHP Nanohybrid Composite

FDA UDI

Class II (US FDA UDI)

by Dental Health Products Inc

Identity

Trade Name
DHP Nanohybrid Composite FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
DHP Nanohybrid Composite Refill A3 20-.25gm Tips FDA UDI
Model / Reference
210-HT40A32 FDA UDI
Description
DHP Nanohybrid Composite Refill A3 20-.25gm Tips FDA UDI

Identifiers

Catalog Number
210-HT40A32 FDA UDI
Primary DI / UDI-DI
D773210HT40A321 FDA UDI
510(k) Number
K130672 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

DHP Nanohybrid Composite by Dental Health Products 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

Sources (1)

  • FDA UDI 64a2bf38-fc9c-4f00-9f1a-b0e414cc6089 36 fields · synced Jun 6, 2026