Identity
- Trade Name
- DENTURE BASE FDA UDI
- Generic Name
- Dental acrylic resin FDA UDI
- Device Name
- DENTURE BASE ORIG. FIB. 1-OZ LIQ&PDR SAMPLE FDA UDI
- Model / Reference
- 072-04-0226 FDA UDI
- Description
- DENTURE BASE ORIG. FIB. 1-OZ LIQ&PDR SAMPLE FDA UDI
Identifiers
- Primary DI / UDI-DI
- D772ATI0402260 FDA UDI
- FDA Product Code
- EMA FDA UDI
- GMDN Term
- Dental acrylic resin FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3275 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dental acrylic resin
Denture Base by American Tooth Industries — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- QUARZ, MDC Dental — MDC DENTAL · Class II
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 |
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Manufacturer
- Manufacturer
- American Tooth Industries
Sources (1)
- FDA UDI ce2d81ac-bfae-47ca-9f96-28ffd708faaa 33 fields · synced Jun 1, 2026