Identity
- Trade Name
- FRAME BASE FDA UDI
- Generic Name
- Temporary dental crown/bridge resin FDA UDI
- Device Name
- FRAME BASE REG. FIBERED 1LB KIT FDA UDI
- Model / Reference
- 072-07-0001 FDA UDI
- Description
- FRAME BASE REG. FIBERED 1LB KIT FDA UDI
Identifiers
- Primary DI / UDI-DI
- D772ATI0700010 FDA UDI
- FDA Product Code
- EMA FDA UDI
- GMDN Term
- Temporary dental crown/bridge 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
Yes
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Temporary dental crown/bridge resin
Frame Base by American Tooth Industries — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 f64001de-a227-4a6e-a713-f4d66e9e0808 33 fields · synced Jun 6, 2026