UF(II) Wide
UF(II) Wide is a titanium screw-form dental implant placed in the bone of the upper or lower jaw. It provides a root-form attachment for single-unit or multiple-unit prostheses. The wide…
UF(II) Wide is a titanium screw-form dental implant placed in the bone of the upper or lower jaw. It provides a root-form attachment for single-unit or multiple-unit prostheses. The wide fixtures are intended for the molar region and delayed loading.
The subject implant bodies are Grade 4 titanium with an SLA surface. Diameters are 5.9, 6.4 and 6.9 mm, with lengths of 7, 8.5, 10, 11.5 or 13 mm. These dimensions distinguish the wide range from smaller implants in the associated product family.
Surgical Sequence and Sterility
Placement uses a conventional two-stage surgical process with an option for transmucosal healing. The fixtures are supplied sterile using gamma irradiation. Immediate-loading indications associated with smaller predicate implants are separate from the delayed-loading use described for the wide fixtures.
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 | DIO Corporation, 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) | K173975 |
| Record published | 2022-03-01 |
| Record revised | 2022-02-28 (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, serial number |
| Storage | Storage environment temperature 1 to 30 °C |
| Distribution end date | 2022-02-28 |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| UF(II) 6508S | In distribution | |
| UF(II) 7007S | In distribution | |
| UF(II) 6011S | In distribution | |
| UF(II) 6511S | In distribution | |
| UF(II) 6510SF | In distribution | |
| UF(II) 7007SF | In distribution | |
| UF(II) 6513S | In distribution | |
| UF(II) 6507SF | In distribution | |
| UF(II) 7010S | In distribution | |
| UF(II) 6510S | In distribution | |
| UF(II) 6511SF | In distribution | |
| UF(II) 7010SF | In distribution | |
| UF(II) 7013SF | In distribution | |
| UF(II) 6508SF | In distribution | |
| UF(II) 6008S | In distribution | |
| UF(II) 6011SF | In distribution | |
| UF(II) 6507S | In distribution | |
| UF(II) 6007S | In distribution | |
| UF(II) 6007SF | In distribution | |
| UF(II) 7011S | In distribution | |
| UF(II) 7008S | In distribution | |
| UF(II) 7008SF | In distribution | |
| UF(II) 6008SF | In distribution | |
| UF(II) 7011SF | In distribution | |
| UF(II) 6013SF | In distribution | |
| UF(II) 6013S | In distribution | |
| UF(II) 6010S | In distribution | |
| UF(II) 7013S | In distribution | |
| UF(II) 6513SF | In distribution | |
| UF(II) 6010SF | In distribution | |
| UF(II) 6507S | Withdrawn | |
| UF(II) 6513SF | Withdrawn | |
| UF(II) 7007S | Withdrawn | |
| UF(II) 6010SF | Withdrawn | |
| UF(II) 7010S | Withdrawn | |
| UF(II) 7010SF | Withdrawn | |
| UF(II) 6007SF | Withdrawn | |
| UF(II) 6007S | Withdrawn | |
| UF(II) 7011S | Withdrawn | |
| UF(II) 6008S | Withdrawn | |
| UF(II) 6511SF | Withdrawn | |
| UF(II) 7011SF | Withdrawn | |
| UF(II) 6011SF | Withdrawn | |
| UF(II) 6508S | Withdrawn | |
| UF(II) 7013S | Withdrawn | |
| UF(II) 7008S | Withdrawn | |
| UF(II) 6510SF | Withdrawn | |
| UF(II) 6507SF | Withdrawn | |
| UF(II) 6013SF | Withdrawn | |
| UF(II) 6011S | Withdrawn | |
| UF(II) 6513S | Withdrawn | |
| UF(II) 6008SF | Withdrawn | |
| UF(II) 6010S | Withdrawn | |
| UF(II) 6508SF | Withdrawn | |
| UF(II) 7007SF | Withdrawn | |
| UF(II) 6013S | Withdrawn | |
| UF(II) 6511S | Withdrawn | |
| UF(II) 7008SF | Withdrawn | |
| UF(II) 6510S | Withdrawn | |
| UF(II) 7013SF | Withdrawn |
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 |
|---|---|
| K182194 | 2018-12-14 |
| K173975 | 2018-06-01 |
| K170608 | 2018-03-30 |
| K161987 | 2017-02-21 |
| K122519 | 2013-05-21 |
| K112746 | 2011-10-21 |
| K100100 | 2010-11-10 |
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.