Identity
- Trade Name
- Basic 6, B1 / U05, CE FDA UDI
- Generic Name
- Resin artificial teeth FDA UDI
- Device Name
- Preformed plastic denture tooth FDA UDI
- Model / Reference
- 56739310 FDA UDI
- Description
- Preformed plastic denture tooth FDA UDI
Identifiers
- Catalog Number
- 56739310 FDA UDI
- Primary DI / UDI-DI
- J014567393100 FDA UDI
- 510(k) Number
- K000213 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Basic 6, B1 / U05, CE by Kulzer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K000213 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 |
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Manufacturer
- Manufacturer
- Kulzer, Inc.
Sources (1)
- FDA UDI 150db72a-177c-4c56-a12b-0c622cae1bd2 37 fields · synced May 31, 2026