Saturno Narrow Diameter Implant System
SATURNO 20° Angled Implant 2.9mmD x 14mmL, 4mm Cuff
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.
| 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
| 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
| 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 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| 07724 | Length 10 mm | Withdrawn |
| 07717 | Length 14 mm | Withdrawn |
| 07704 | Length 12 mm | Withdrawn |
| 07720 | Length 14 mm | Withdrawn |
| 07716 | Length 12 mm | Withdrawn |
| 07725 | Length 12 mm | Withdrawn |
| 07729 | Length 14 mm | Withdrawn |
| 07735 | Length 14 mm | Withdrawn |
| 07706 | Length 10 mm | Withdrawn |
| 07723 | Length 14 mm | Withdrawn |
| 07709 | Length 10 mm | Withdrawn |
| 07711 | Length 14 mm | Withdrawn |
| 07719 | Length 12 mm | Withdrawn |
| 07727 | Length 10 mm | Withdrawn |
| 07707 | Length 12 mm | Withdrawn |
| 07701 | Length 12 mm | Withdrawn |
| 07721 | Length 10 mm | Withdrawn |
| 07715 | Length 10 mm | Withdrawn |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
| 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
| 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.
| 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.
| 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.