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
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Cleared under the same submission
K130672 also covers:
- DHP Nanohybrid Composite — Dental Health Products Inc
- DHP Nanohybrid Composite — Dental Health Products Inc
- DHP Nanohybrid Composite — Dental Health Products Inc
- DHP Nanohybrid Composite — Dental Health Products Inc
- DHP Nanohybrid Composite — Dental Health Products Inc
- DHP Nanohybrid Composite — Dental Health Products Inc
- DHP Nanohybrid Composite — Dental Health Products Inc
- DHP Nanohybrid Composite — Dental Health Products Inc
- DHP Nanohybrid Composite — Dental Health Products Inc
- DHP Nanohybrid Composite — Dental Health Products Inc
- DHP Nanohybrid Composite — Dental Health Products Inc
- DHP Nanohybrid Composite — Dental Health Products Inc
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Dental Health Products Inc
Sources (1)
- FDA UDI 64a2bf38-fc9c-4f00-9f1a-b0e414cc6089 36 fields · synced Jun 6, 2026