2 catalogue numbers from 300755, listed by CeramTec Schweiz GmbH, Switzerland, under Implant, Endosseous, Root-Form. 7 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Jiangsu (3), Sichuan (2), Shanghai (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
Record
Regulatory record for NobelPearl Tapered RP 4.2x8mm | Listed by | CeramTec Schweiz GmbH, Switzerland |
| FDA product code | DZE |
| Device type | Implant, Endosseous, Root-Form |
| Device class | Class 2 |
| Regulation | 21 CFR 872.3640 |
| Establishment | Manufacturer |
| 510(k) | K180184 |
| Record published | 2021-10-26 |
| Record revised | 2026-07-03 (version 3) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Storage | Special storage condition: Keep dry, Keep out of sunlight; Storage environment temperature 15 to 25 °C |
| Distribution end date | 2026-07-02 |
| UDI direct marking | Exempt |
PMA Approvals
A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.