SPI Element Inicell

70 catalogue numbers from 4.23.141, listed by Thommen Medical, AG, Switzerland, under Implant, Endosseous, Root-Form. 7 manufacturers in China are registered for this product code.

Registry build 21.09.26
7manufacturers in China registered for this device type
70catalogue numbers in this listing
9510(k) clearances naming this product code
1recall

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 SPI Element Inicell
Listed by Thommen Medical, AG, Switzerland
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Manufacturer
510(k) K090154
Record published 2015-09-24
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for SPI Element Inicell
Catalogue number Size Status
4.23.141 In distribution
4.23.115 In distribution
4.23.522 In distribution
4.23.126 In distribution
4.23.145 In distribution
4.23.112 In distribution
4.23.133 In distribution
4.23.535 In distribution
4.23.544 In distribution
4.23.724 In distribution
4.23.131 In distribution
4.23.117 In distribution
4.23.132 In distribution
4.23.142 In distribution
4.23.552 In distribution
4.23.135 In distribution
4.23.114 In distribution
4.23.514 In distribution
4.23.102 In distribution
4.23.146 In distribution
4.23.137 In distribution
4.23.533 In distribution
4.23.546 In distribution
4.23.105 In distribution
4.23.153 In distribution
4.23.542 In distribution
4.23.555 In distribution
4.23.712 In distribution
4.23.524 In distribution
4.23.553 In distribution
4.23.143 In distribution
4.23.513 In distribution
4.23.726 In distribution
4.23.512 In distribution
4.23.716 In distribution
4.23.526 In distribution
4.23.516 In distribution
4.23.136 In distribution
4.23.714 In distribution
4.23.134 In distribution
4.23.725 In distribution
4.23.113 In distribution
4.23.155 In distribution
4.23.721 In distribution
4.23.715 In distribution
4.23.151 In distribution
4.23.124 In distribution
4.23.723 In distribution
4.23.534 In distribution
4.23.125 In distribution
4.23.525 In distribution
4.23.104 In distribution
4.23.122 In distribution
4.23.121 In distribution
4.23.103 In distribution
4.23.543 In distribution
4.23.713 In distribution
4.23.116 In distribution
4.23.144 In distribution
4.23.523 In distribution
4.23.532 In distribution
4.23.554 In distribution
4.23.545 In distribution
4.23.515 In distribution
4.23.106 In distribution
4.23.123 In distribution
4.23.722 In distribution
4.23.536 In distribution
4.23.154 In distribution
4.23.152 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
K171795 2017-09-29
K093615 2010-03-04
K090154 2009-07-27
K072649 2007-12-06
K072933 2007-11-15
K070007 2007-01-10
K051502 2005-06-21
K034014 2004-03-05
K030689 2003-03-26

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2007-04-19 Not classified Other The undercut on the SPI EASY abutments which engages the stabilization ring of the implant is missing. Although the abutments can still be placed on the implant by the user the parts do not fulfill the quality expectations of the firm. 84 2008-05-12

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