Inverta®

INVERTA®, Ø4.2 ExHex 12° CO-AXIS®, Ø5.0 x 11.5mm

Registry build 21.09.26
7manufacturers in China registered for this device type
59catalogue numbers in this listing
17510(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 Inverta®
Listed by Southern Implants (PTY) Ltd, South Africa
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Manufacturer, Exporter
510(k) K181850
Record published 2021-11-22
Record revised 2022-09-06 (version 2)

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 Inverta®
Catalogue number Size Status
IV-EX4012D-5018 In distribution
IV-DC34-3913 In distribution
IV-EX4012D-5013 In distribution
IV-DC4012D-5011 In distribution
IV-DC35-4518 In distribution
IV-EX3512D-4513 In distribution
IV-EX52-6011 In distribution
IV-EX5212D-6013 In distribution
IV-DC50-6010 In distribution
IV-DC4012D-5013 In distribution
IV-EX4212D-5018 In distribution
IV-EX35-4518 In distribution
IV-EX35-4511 In distribution
IV-EX4212D-5015 In distribution
IV-DC34-3915 In distribution
IV-DC50-6011 In distribution
IV-DC40-5018 In distribution
IV-DC4012D-5015 In distribution
IV-EX3512D-4518 In distribution
IV-EX52-6018 In distribution
IV-EX35-4513 In distribution
IV-EX40-5015 In distribution
IV-DC35-4511 In distribution
IV-DC35-4510 In distribution
IV-EX4212D-5011 In distribution
IV-DC35-4513 In distribution
IV-DC50-6015 In distribution
IV-DC4012D-5018 In distribution
IV-DC50-6013 In distribution
IV-EX4212D-5013 In distribution
IV-EX3512D-4511 In distribution
IV-EX3512D-4515 In distribution
IV-EX4012D-5015 In distribution
IV-DC3512D-4511 In distribution
IV-DC34-3910 In distribution
IV-EX5212D-6015 In distribution
IV-DC34-3911 In distribution
IV-DC40-5011 In distribution
IV-EX40-5011 In distribution
IV-DC3512D-4513 In distribution
IV-DC35-4515 In distribution
IV-DC50-6018 In distribution
IV-EX40-5010 In distribution
IV-EX35-4510 In distribution
IV-EX5212D-6011 In distribution
IV-EX40-5013 In distribution
IV-EX40-5018 In distribution
IV-DC40-5010 In distribution
IV-DC3512D-4518 In distribution
IV-EX5212D-6018 In distribution
IV-DC40-5013 In distribution
IV-DC40-5015 In distribution
IV-EX52-6010 In distribution
IV-EX35-4515 In distribution
IV-EX52-6013 In distribution
IV-EX52-6015 In distribution
IV-DC35-4508 In distribution
IV-EX4012D-5011 In distribution
IV-DC40-5008 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
K232726 2024-04-01
K232418 2023-12-01
K222457 2023-03-06
K222497 2022-11-09
K192651 2020-05-07
K191054 2019-12-09
K181850 2018-11-14
K180465 2018-09-06
K173706 2018-06-08
K173343 2018-02-27
K163634 2017-11-06
K163060 2017-06-13
K093562 2010-10-14
K082651 2008-12-22
K071161 2007-11-16
K070841 2007-06-21
K070905 2007-05-24

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. 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
2015-01-23 Class II Mixed-up of materials/components Z-MAX Implant, 9mm diameter, 7mm length labeled package, catalog number Z-MAX9-7, contained a MAX-TL Implant, 9mm diameter, 7mm length. And vice versa. 130 units 2015-05-20

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