Saturno Narrow Diameter Implant System

SATURNO 20° Angled Implant 2.9mmD x 14mmL, 4mm Cuff

Registry build 21.09.26
7manufacturers in China registered for this device type
36catalogue numbers in this listing
8510(k) clearances naming this product code
3recalls on this 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 Saturno Narrow Diameter Implant System
Listed by Zest Anchors, 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, Repacker / relabeller, Manufacturer
Record published 2016-02-16
Record revised 2026-05-19 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Radiation Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Sizes Length 10 to 14 mm
Distribution end date 2026-05-18
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Saturno Narrow Diameter Implant System
Catalogue number Size Status
07702 Length 14 mm In distribution
07724 Length 10 mm Withdrawn
07717 Length 14 mm Withdrawn
07704 Length 12 mm Withdrawn
07720 Length 14 mm Withdrawn
07716 Length 12 mm Withdrawn
07725 Length 12 mm Withdrawn
07729 Length 14 mm Withdrawn
07735 Length 14 mm Withdrawn
07706 Length 10 mm Withdrawn
07723 Length 14 mm Withdrawn
07709 Length 10 mm Withdrawn
07711 Length 14 mm Withdrawn
07719 Length 12 mm Withdrawn
07727 Length 10 mm Withdrawn
07707 Length 12 mm Withdrawn
07701 Length 12 mm Withdrawn
07721 Length 10 mm Withdrawn
07715 Length 10 mm Withdrawn
07731 Length 12 mm Withdrawn
07722 Length 12 mm Withdrawn
07733 Length 10 mm Withdrawn
07728 Length 12 mm Withdrawn
07718 Length 10 mm Withdrawn
07726 Length 14 mm Withdrawn
07713 Length 12 mm Withdrawn
07714 Length 14 mm Withdrawn
07710 Length 12 mm Withdrawn
07703 Length 10 mm Withdrawn
07712 Length 10 mm Withdrawn
07734 Length 12 mm Withdrawn
07708 Length 14 mm Withdrawn
07705 Length 14 mm Withdrawn
07700 Length 10 mm Withdrawn
07730 Length 10 mm Withdrawn
07732 Length 14 mm 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
K133327 2014-06-25
K120198 2012-06-06
K033699 2004-04-22
K994257 2000-03-17
K925849 1994-11-18
K934668 1994-06-22
K840244 1984-05-01
K801524 1980-07-21

Recalls

2 of these are 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
2019-11-22 Class II Process control The abutment provided with the Implant System may be out of specification, which could lead to a small gap occurring between the implant and abutment on assembly in the patient. 154 kits
2014-01-16 Class II Unknown/Undetermined by firm Zest Anchors, LLC is voluntarily recalling specific lots of LOCATOR Implant Attachment Systems because it is currently provided with a label that indicates that the final torque applied to the abutment should be 30 N-cm. It was recently not 3,130 2014-05-15
2008-04-09 Not classified Nonconforming Material/Component The recall was initiated after the firm discovered through a customer complaint that the Locator Abutments for 5.7 Screw-vent & Compatibles do not fit properly in all sizes of the Zimmer Dental 5.7mm diameter Tapered Screw-Vent Implants (TS 996 units 2008-12-02

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