Versalis S Plus

IMP. Versalis S Plus MT16° Ø4.0X11.5MM

Registry build 21.09.26
7manufacturers in China registered for this device type
47catalogue numbers in this listing

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 Versalis S Plus
Listed by SIN Sistema DE Implante Nacional S.A
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Record published 2025-08-18

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Versalis S Plus
Catalogue number Size Status
IVMT 4011N In distribution
IVMT 3818N In distribution
IVMT 3815N In distribution
IVMT 4013N In distribution
IVMT 3824N In distribution
IVMT 3820N In distribution
IVMT 3510N In distribution
IVMT 5085N In distribution
IVMT 6085N In distribution
IVMT 4022N In distribution
IVMT 7013N In distribution
IVMT 5011N In distribution
IVMT 5013N In distribution
IVMT 3511N In distribution
IVMT 4318N In distribution
IVMT 4085N In distribution
IVMT 7010N In distribution
IVMT 3810N In distribution
IVMT 4015N In distribution
IVMT 3518N In distribution
IVMT 6010N In distribution
IVMT 3885N In distribution
IVMT 4324N In distribution
IVMT 3585N In distribution
IVMT 3811N In distribution
IVMT 4313N In distribution
IVMT 4018N In distribution
IVMT 4311N In distribution
IVMT 3822N In distribution
IVMT 3513N In distribution
IVMT 4322N In distribution
IVMT 6013N In distribution
IVMT 7085N In distribution
IVMT 6011N In distribution
IVMT 3515N In distribution
IVMT 4024N In distribution
IVMT 4385N In distribution
IVMT 4315N In distribution
IVMT 5010N In distribution
IVMT 4320N In distribution
IVMT 4010N In distribution
IVMT 3813N In distribution
IVMT 4020N In distribution
IVMT 7011N In distribution
IVMT 4310N In distribution
IVMT 5018N In distribution
IVMT 5015N 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

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