Identity
- Trade Name
- Tokuso Rebase MR Bond FDA UDI
- Generic Name
- Denture reliner, hard FDA UDI
- Model / Reference
- 20133 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04548190201334 FDA UDI
- 510(k) Number
- K973245 FDA UDI
- FDA Product Code
- KLE FDA UDI
- GMDN Term
- Denture reliner, hard FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3200 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Denture reliner, hard
Tokuso Rebase MR Bond by Tokuyama Dental Corporation — 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
- Tokuyama Dental Corporation
Sources (1)
- FDA UDI aaf8a0c4-638a-4b37-9677-a07ceabbe8b1 35 fields · synced May 30, 2026