Biotanium

4.3mm X 11.5mm Implant & Healing Screw

Registry build 21.09.26
7manufacturers in China registered for this device type
46catalogue numbers in this listing
6510(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 Biotanium
Listed by Basic Dental Implant Systems, Inc., United States
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Repacker / relabeller, Manufacturer
510(k) K082749
Record published 2023-09-21

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date, serial number
Distribution end date 2026-04-20

Catalogue Numbers

Catalogue numbers for Biotanium
Catalogue number Size Status
B43115S In distribution
O6008S In distribution
O4513S In distribution
B35115S In distribution
B43145S In distribution
B5013S In distribution
O4515S In distribution
B4385S In distribution
O5011S In distribution
O6010S In distribution
O3515S In distribution
O5015S In distribution
B4316S In distribution
O3513PW In distribution
O5013S In distribution
B4310S In distribution
O4011S In distribution
B50115S In distribution
O6013S In distribution
B5085S In distribution
B35145S In distribution
O4511S In distribution
O4013S In distribution
B3585S In distribution
B3516S In distribution
B4313S In distribution
O3513S In distribution
O6015S In distribution
B3510S In distribution
O4015S In distribution
OT104 In distribution
O4011PW In distribution
B3513S In distribution
O6012S In distribution
B50145S In distribution
O5009S In distribution
O3515PW In distribution
O3511S In distribution
O4509S In distribution
O6011S In distribution
O3511PW In distribution
B5010S In distribution
OT105 In distribution
OT140 Withdrawn
OT101 Withdrawn
OT139 Withdrawn

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
K082749 2008-12-04
K072595 2008-05-09
K022912 2002-09-20
K013682 2001-11-28
K012299 2001-08-01
K001259 2001-01-12

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