Versatile Implant

Ø3.75mm x L11.5mm, Conical Connection, Regular Platform

Registry build 21.09.26
7manufacturers in China registered for this device type
64catalogue numbers in this listing
2510(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 Versatile Implant
Listed by Surgikor, LLC, United States
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Specification developer, Manufacturer
510(k) K152555
Record published 2017-01-31
Record revised 2024-09-19 (version 4)

Specifications

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, serial number

Catalogue Numbers

Catalogue numbers for Versatile Implant
Catalogue number Size Status
VRH6013 In distribution
VRH4508 In distribution
VRH6008 In distribution
VRH3508 In distribution
VRH4220 In distribution
VWC4213 In distribution
VRH6010 In distribution
VWC6016 In distribution
VWC5016 In distribution
VRH6011 In distribution
VRH4510 In distribution
VRH5013 In distribution
VRC3711 In distribution
VWC5010 In distribution
VRH4516 In distribution
VRC3710 In distribution
VRH3516 In distribution
VWC6013 In distribution
VRH4513 In distribution
VWC4508 In distribution
VWC4218 In distribution
VRC3713 In distribution
VRH3708 In distribution
VWC4511 In distribution
VRH3716 In distribution
VWC4513 In distribution
VWC6011 In distribution
VRH3710 In distribution
VRH5016 In distribution
VRC3508 In distribution
VRH3711 In distribution
VWC5011 In distribution
VRH5008 In distribution
VWC4216 In distribution
VWC4210 In distribution
VRH4211 In distribution
VRC3708 In distribution
VRH5010 In distribution
VWC4516 In distribution
VRH3511 In distribution
VRH4511 In distribution
VRH4208 In distribution
VRC3716 In distribution
VRH4213 In distribution
VWC5013 In distribution
VWC4510 In distribution
VRH4218 In distribution
VWC6010 In distribution
VRH4210 In distribution
VRC3510 In distribution
VRH3510 In distribution
VRH6016 In distribution
VWC4211 In distribution
VWC4220 In distribution
VRH3513 In distribution
VRH3513 In distribution
VRC3511 In distribution
VRC3516 In distribution
VWC4208 In distribution
VWC6008 In distribution
VRH5011 In distribution
VWC5008 In distribution
VRH4216 In distribution
VRC3513 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
K240803 2024-09-12
K182615 2019-07-08

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