KDF Zirconia Disc MU-A2/10mm
by Denken-Highdental Co., Ltd. GUDID
Listed
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04560230233990 | Date11 Aug 2023 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 23 Oct 2026.
Specification
- Trade Name
- KDF Zirconia Disc
- Generic Name
- Dental appliance fabrication material, ceramic
- Model / Reference
- MU-A2/10mm
- Primary DI / UDI-DI
- 04560230233990
- 510(k) Number
- FDA Product Code
- EIH
- GMDN Term
- Dental appliance fabrication material, ceramic
- Device Class
- Class II
- Regulation Number
- 872.6660
- GUDID distribution status
- In Commercial Distribution
Other devices from Denken-Highdental Co., Ltd.
Properties
Other properties (10)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No