S-Clean SQ-SL Implant System Mini
The s-Clean SQ-SL Mini fixture is a threaded dental implant for the upper or lower jaw. It supports single or multiple tooth restorations in partially or fully edentulous jaws and is…
The s-Clean SQ-SL Mini fixture is a threaded dental implant for the upper or lower jaw. It supports single or multiple tooth restorations in partially or fully edentulous jaws and is intended for delayed loading through one or two stage surgery.
The fixture is made from commercially pure titanium with a sandblasted and acid etched surface. Its internal hexagonal interface resists rotation and connects to the specified S-Line prosthetic abutments.
Listed Item
Dental Implant System / s-Clean SQ-SL Fixture Mini (DSSFM3510)
Connection System
The implant body has upper and lower screw joints. The compatible S-Line abutments use the upper connection with a 2.0 mm screw. Separate cover screws protect the connection during healing, while the final abutment supports the planned prosthesis.
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 | Dentis Co., Ltd., South Korea |
|---|---|
| FDA product code | DZE |
| Device type | Implant, Endosseous, Root-Form |
| Device class | Class 2 |
| Regulation | 21 CFR 872.3640 |
| Establishment | Manufacturer, Exporter |
| 510(k) | K202773 |
| Record published | 2022-06-17 |
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, manufacturing date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| DSSFM3510 | In distribution | |
| DSSFM4010 | In distribution | |
| DSSFM3512 | 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 |
|---|---|
| K253493 | 2026-03-04 |
| K240511 | 2024-05-20 |
| K210080 | 2021-06-04 |
| K210134 | 2021-04-19 |
| K202773 | 2021-03-18 |
| K210132 | 2021-02-17 |
| K200099 | 2020-04-13 |
| K192688 | 2020-02-04 |
| K171027 | 2017-09-06 |
| K170220 | 2017-04-27 |
| K161244 | 2016-12-07 |
| K160213 | 2016-06-21 |
| K153639 | 2016-04-08 |
| K142313 | 2015-12-10 |
| K150344 | 2015-07-24 |
| K111364 | 2012-02-01 |
| K082843 | 2009-06-19 |
| K083586 | 2009-04-29 |
| K073486 | 2008-04-04 |
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.