Abutment Screw
The MegaGen Abutment Screw secures a dental abutment to an endosseous implant. It is a prosthetic connection component of the BLUEDIAMOND implant system, rather than the implant fixture…
The MegaGen Abutment Screw secures a dental abutment to an endosseous implant. It is a prosthetic connection component of the BLUEDIAMOND implant system, rather than the implant fixture placed in bone.
The screw is made from Ti-6Al-4V ELI titanium alloy. Its M1.6 connection is used with specified MegaGen abutments, including EZ Post, angled, milling, CCM, temporary and Fuse abutments.
Listed Item
BLUEDIAMOND IMPLANT System M1.6/ Long
Compatible Restoration System
BLUEDIAMOND fixtures provide support for crowns, bridges and overdentures in partially or fully edentulous patients. The system is intended for the molar regions of the upper or lower jaw, and the screw must match the selected compatible implant and abutment.
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.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 54 |
| LX Precision Shanghai Co Ltd | Shanghai | Shanghai | Contract manufacturer | 19 |
| Jiangsu Trausim Medical Instrument Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 3 |
| Basic (Chengdu) Medical Device Co., Ltd. | Chengdu | Sichuan | Contract manufacturer | 1 |
| Dongguan Xinlonghong Hardware Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 1 |
| Chengdu Besmile Medical Technology Co., Ltd. | Chengdu | Sichuan | Manufacturer | 14 |
| BIO Concept Co., Ltd. | Changzhou | Jiangsu | Manufacturer | 5 |
Record
| Listed by | Megagen Implant Co., Ltd., South Korea |
|---|---|
| FDA product code | DZE |
| Device type | Implant, Endosseous, Root-Form |
| Device class | Class 2 |
| Regulation | 21 CFR 872.3640 |
| Establishment | Repacker / relabeller, Manufacturer, Exporter |
| 510(k) | K211812 |
| Record published | 2023-06-20 |
| Record revised | 2026-03-25 (version 2) |
Specifications
| MRI safety | MR Conditional |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, manufacturing date, serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| AROAS16L | In distribution | |
| AROAS16BL | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Neodent | Jjgc Indústria e Comércio de Materiais Dentários S.A. | 920 |
| Osstem Implant System | Osstem Implant Co., Ltd. | 788 |
| Magicore | InnoBioSurg Co., Ltd.(IBS implant Co., Ltd.) | 744 |
| Implant, Endosseous, Root-Form | Southern Implants (PTY) Ltd | 608 |
| ITL Dental | Emery Enterprises Inc. | 603 |
| Magicore S | InnoBioSurg Co., Ltd.(IBS implant Co., Ltd.) | 560 |
| Friadent® | Dentsply Implants Manufacturing GmbH | 525 |
| Sphero Block Normo | Rhein 83 SRL | 489 |
| Neobiotech Implant System | Neobiotech Co., Ltd. | 483 |
| KJ Mini Implant System | Kjmeditech.co., Ltd. | 448 |
| Ritter Dental Implant System | Ritter Implants GmbH & Co. KG | 418 |
| Leone SPA | Leone SPA | 404 |
Showing 12 of 2,762. All products under Implant, Endosseous, Root-Form
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K251232 | 2026-06-18 |
| K241972 | 2024-12-27 |
| K231967 | 2023-12-07 |
| K230618 | 2023-10-11 |
| K223339 | 2023-07-18 |
| K211812 | 2023-01-06 |
| K203554 | 2021-08-28 |
| K210161 | 2021-06-22 |
| K192347 | 2019-11-14 |
| K182448 | 2019-10-09 |
| K191127 | 2019-10-08 |
| K150537 | 2015-07-21 |
| K140091 | 2014-12-12 |
| K123988 | 2013-08-15 |
| K123870 | 2013-03-27 |
| K122231 | 2012-10-04 |
| K081302 | 2008-08-15 |
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.
| PMA number | Decision | Trade name | Approved to |
|---|---|---|---|
| P800035 | 2001-10-04 | PERI-OSS | Curasan AG |
| P860012 | 1988-10-28 | ALVEOFORM TM BIOGRAFT | Collagen Corp. |
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.