Kenson T18C2U0L30
by The Myerson Company Limited
Ref T18C2U0L30
Active
CE MDR
Valid until
16 Oct 2030
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number08423261TeethXK 00842326121768 | Date19 Nov 2025 | StatusActive |
| United States | GUDID listing GUDID | Number00842326121768 | Date24 Sep 2016 | StatusListed |
Certificates
- 28620225594 Active
Quality management system EU MDR
- Certifier
- Intertek Medical Notified Body AB 2862
- Issued
- 17 Oct 2025
- Expires
- 16 Oct 2030
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Kenson
- Generic Name
- Resin artificial teeth
- Device Name
- Preformed Artificial Teeth
- Model / Reference
- T18C2U0L30
- Primary DI / UDI-DI
- 00842326121768
- Basic UDI-DI
- 08423261TeethXK
- 510(k) Number
- FDA Product Code
- ELM
- EMDN Code
- P01020101 Dental implants
- GMDN Term
- Resin artificial teeth
- Device Class
- Class IIa EUDAMEDClass II GUDID
- Regulation Number
- 872.3590
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIa | Class II |
| Implantable | Yes | No |
Other devices from The Myerson Company Limited
Properties
Other properties (21)
- Sterile: No
- Single Use: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No