Identity
- Trade Name
- ODIPAL FDA UDI
- Generic Name
- Resin artificial teeth FDA UDI
- Device Name
- ODIPAL anterior Teeth Shade A4 , Mould U16 FDA UDI
- Model / Reference
- ANTERIOR TEETH A4/U16 FDA UDI
- Description
- ODIPAL anterior Teeth Shade A4 , Mould U16 FDA UDI
Identifiers
- Catalog Number
- D2A4U16 FDA UDI
- Primary DI / UDI-DI
- 08435288421865 FDA UDI
- 510(k) Number
- K070591 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
- 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Resin artificial teeth
The ODIPAL dental device is a high-quality, prefabricated resin artificial teeth made of polymer-based material for mounting on dentures. It features a durable design and is suitable for individuals seeking a cost-effective alternative to traditional metal implants.
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Also classified as Resin artificial teeth.
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Cleared under the same submission
K070591 also covers:
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
- Union Dental Sa
Sources (1)
- FDA UDI 2cbc89e3-6bc3-4b70-9d8e-b42f885ccd1a 35 fields · synced Jul 15, 2026