Kisses Mini Internal Fixture
The Kisses Mini Internal Fixture is a dental implant placed in the jawbone to support a replacement tooth. The 3.2 mm internal hex fixture is indicated for replacement of upper lateral…
The Kisses Mini Internal Fixture is a dental implant placed in the jawbone to support a replacement tooth. The 3.2 mm internal hex fixture is indicated for replacement of upper lateral incisors and lower incisors in patients with missing teeth.
The fixture has a threaded body for fixation in bone, a self-tapping cutting edge and an internal hex connection for the prosthetic component. It is made from grade 4 titanium with a sandblasted and acid-etched surface.
Listed Item
Kisses Mini Internal Fixture Φ3.2/L14.5
Placement and Loading
The fixture is intended for single-stage or two-stage surgical procedures with delayed loading. It is supplied sterile following gamma sterilization.
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 | Achimhai Medical Corporation, South Korea |
|---|---|
| FDA product code | DZE |
| Device type | Implant, Endosseous, Root-Form |
| Device class | Class 2 |
| Regulation | 21 CFR 872.3640 |
| 510(k) | K170394 |
| Record published | 2017-11-30 |
| Record revised | 2018-07-06 (version 3) |
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 |
| Storage | Storage environment temperature 1 to 30 °C |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| MFX-3215SD | In distribution | |
| MFX-3208S | In distribution | |
| MFX-3208SD | In distribution | |
| MFX-3213SD | In distribution | |
| MFX-3210SD | In distribution | |
| MFX-3211S | In distribution | |
| MFX-3208SD | In distribution | |
| MFX-3211SD | In distribution | |
| MFX-3215S | In distribution | |
| MFX-3208S | In distribution | |
| MFX-3215SD | In distribution | |
| MFX-3210SD | In distribution | |
| MFX-3213S | In distribution | |
| MFX-3211S | In distribution | |
| MFX-3210S | In distribution | |
| MFX-3211SD | In distribution | |
| MFX-3213SD | In distribution | |
| MFX-3210S | In distribution | |
| MFX-3215S | In distribution | |
| MFX-3213S | 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 |
|---|---|
| K172630 | 2018-04-03 |
| K170394 | 2017-10-06 |
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.