Identity
- Trade Name
- Dymon-Hue Posterior Teeth 1x8 Perforated Cards FDA UDI
- Generic Name
- Resin artificial teeth FDA UDI
- Device Name
- Dymon-Hue Posterior Hardened Plastic Teeth 1x8 Perforated Cards FDA UDI
- Model / Reference
- 082-19974/P FDA UDI
- Description
- Dymon-Hue Posterior Hardened Plastic Teeth 1x8 Perforated Cards FDA UDI
Identifiers
- Catalog Number
- 082-19974/P FDA UDI
- Primary DI / UDI-DI
- D772ATI19974P0 FDA UDI
- FDA Product Code
- ELM FDA UDI
- GMDN Term
- Resin artificial teeth FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3590 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dymon-Hue Posterior Teeth 1x8 Perforated Cards by American Tooth Industries — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- American Tooth Industries
Sources (1)
- FDA UDI 862e9e40-48a8-4e8e-805d-8a1caf735780 35 fields · synced May 31, 2026