NB II Fixture

The FDA filing identifies the NB II Fixture as the fixture component of the NB Implant System. It describes the fixture as the portion implanted into bone that connects prosthetic devices…

Registry build 21.09.26

The FDA filing identifies the NB II Fixture as the fixture component of the NB Implant System.

It describes the fixture as the portion implanted into bone that connects prosthetic devices or other dental implant components with the mandible or maxilla.

System Context

The NB Implant System is intended to support single or multiple-unit restorations, including cement-retained, screw-retained, or overdenture restorations. The filing also describes an SLA-treated fixture surface and pure titanium material.

7manufacturers in China registered for this device type
60catalogue numbers in this listing
7510(k) clearances naming this product code

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.

Chinese manufacturers registered for FDA product code DZE
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

Regulatory record for NB II Fixture
Listed by Arum Dentistry 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
510(k) K230725
Record published 2023-07-05

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for NB II Fixture
Catalogue number Size Status
NB25507SS In distribution
NB26513SP In distribution
NB26513SS In distribution
NB25010SS In distribution
NB25007SP In distribution
NB25510SS In distribution
NB24508SS In distribution
NB26011SS In distribution
NB26013SP In distribution
NB24507SP In distribution
NB24008SP In distribution
NB24008SS In distribution
NB24013SS In distribution
NB25008SS In distribution
NB24510SS In distribution
NB26511SS In distribution
NB25511SS In distribution
NB25013SS In distribution
NB25507SP In distribution
NB25510SP In distribution
NB25008SP In distribution
NB24510SP In distribution
NB26010SS In distribution
NB26008SS In distribution
NB25513SP In distribution
NB26508SP In distribution
NB25007SS In distribution
NB24513SS In distribution
NB25011SP In distribution
NB26510SS In distribution
NB24011SP In distribution
NB26510SP In distribution
NB24011SS In distribution
NB25010SP In distribution
NB25513SS In distribution
NB26507SP In distribution
NB26507SS In distribution
NB25011SS In distribution
NB24007SP In distribution
NB24010SP In distribution
NB25508SS In distribution
NB26010SP In distribution
NB26511SP In distribution
NB24013SP In distribution
NB26008SP In distribution
NB26007SP In distribution
NB26007SS In distribution
NB26508SS In distribution
NB24513SP In distribution
NB26011SP In distribution
NB24508SP In distribution
NB24511SP In distribution
NB24007SS In distribution
NB25013SP In distribution
NB24507SS In distribution
NB26013SS In distribution
NB24511SS In distribution
NB24010SS In distribution
NB25508SP In distribution
NB25511SP In distribution

Same Product Code

Other products under the same FDA 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

FDA 510(k) clearances naming this product code
Clearance Decision date
K250280 2025-07-23
K241703 2025-02-24
K242753 2025-01-06
K240091 2024-04-26
K230725 2023-07-01
K222131 2022-09-19
K213506 2022-04-06

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.

FDA premarket approvals naming this product code
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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer