Small Diameter Implant System
Bone Level Tapered Implant, Ø 2.9mm SC, SLActive® 14mm, Roxolid®, Loxim™
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 | Institut Straumann AG, Switzerland |
|---|---|
| FDA product code | DZE |
| Device type | Implant, Endosseous, Root-Form |
| Device class | Class 2 |
| Regulation | 21 CFR 872.3640 |
| Establishment | Specification developer, Complaint-file establishment, Manufacturer, Exporter |
| Record published | 2019-04-26 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Storage | Special storage condition: Keep away from sunlight |
| Sizes | Outer diameter 2.9 mm; length 10 to 14 mm |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| SLActive Roxolid BL | Outer Diameter 2.9 mm | In distribution |
| SLActive Roxolid BL | Length 10 mm | In distribution |
| SLA Roxolid BL | Length 14 mm | In distribution |
| SLA Roxolid BL | Outer Diameter 2.9 mm | In distribution |
| SLActive Roxolid BL | Outer Diameter 2.9 mm | 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 |
|---|---|
| K252168 | 2026-03-10 |
| K250294 | 2025-08-12 |
| K241391 | 2024-12-10 |
| K234049 | 2024-03-20 |
| K230108 | 2023-09-14 |
| K223083 | 2023-06-22 |
| K212533 | 2022-01-28 |
| K211052 | 2021-07-08 |
| K210855 | 2021-06-21 |
| K200586 | 2020-08-20 |
| K191256 | 2019-12-27 |
| K191895 | 2019-12-09 |
| K180477 | 2019-01-04 |
| K181703 | 2018-12-28 |
| K173961 | 2018-06-05 |
| K153758 | 2016-03-23 |
| K081419 | 2009-02-20 |
| K062129 | 2006-10-20 |
| K061176 | 2006-08-11 |
| K053088 | 2006-02-27 |
| K033984 | 2004-06-30 |
| K033922 | 2004-01-07 |
| K020096 | 2002-02-08 |
| K013891 | 2002-02-05 |
| K013798 | 2001-12-19 |
| K003552 | 2001-08-17 |
| K003271 | 2001-03-20 |
| K983742 | 1999-03-15 |
| K894595 | 1990-02-13 |
| K894594 | 1990-02-13 |
| K894593 | 1990-02-13 |
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.