Salvation 3di

72 catalogue numbers from SP225555, listed by Wright Medical Technology, Inc., United States, under Plate, Fixation, Bone. 22 manufacturers in China are registered for this product code.

Registry build 21.09.26
22manufacturers in China registered for this device type
72catalogue numbers in this listing
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (4), Zhejiang (3). 12 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HRS
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Kingj Medical Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Hangzhou Sino-MIM Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5
Beijing AK Medical Co., Ltd. Changping District Beijing Contract manufacturer 3

Showing 12 of 22. All 22 manufacturers in China registered for Plate, Fixation, Bone

Record

Regulatory record for Salvation 3Di
Listed by Wright Medical Technology, Inc., United States
FDA product code HRS
Device type Plate, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-10-01
Record revised 2024-02-19 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number, manufacturing date
Sizes Length 16 to 60 mm; outer diameter 4 to 5.5 mm

Catalogue Numbers

Catalogue numbers for Salvation 3Di
Catalogue number Size Status
SP225555 Length 55 mm In distribution
SP225518 Locking In distribution
SP225545 Outer Diameter 5.5 mm In distribution
SP235530 Outer Diameter 5.5 mm In distribution
SP235532 Outer Diameter 5.5 mm In distribution
SP01002L Size: Small In distribution
SP225536 Locking In distribution
SP01002R Size: Small In distribution
SP235540 Outer Diameter 5.5 mm In distribution
SP234025 Length 25 mm In distribution
SP225525 Outer Diameter 5.5 mm In distribution
SP02004L Left In distribution
SP234018 Outer Diameter 4 mm In distribution
SP02003L Left In distribution
SP224040 Outer Diameter 4 mm In distribution
SP234060 Outer Diameter 4 mm In distribution
SP225540 Length 40 mm In distribution
SP02002L Size: Small In distribution
SP234050 Outer Diameter 4 mm In distribution
SP01003R Size: Medium In distribution
SP235525 Length 25 mm In distribution
SP02001L Extra Small, Left In distribution
SP224045 Locking In distribution
SP235545 Length 45 mm In distribution
SP235555 Length 55 mm In distribution
SP224016 Outer Diameter 4 mm In distribution
SP224038 Locking In distribution
SP224060 Length 60 mm In distribution
SP225530 Outer Diameter 5.5 mm In distribution
SP225520 Length 20 mm In distribution
SP02004R Right In distribution
SP234040 Outer Diameter 4 mm In distribution
SP235550 Length 50 mm In distribution
SP224025 Locking In distribution
SP225516 Outer Diameter 5.5 mm In distribution
SP234016 Length 16 mm In distribution
SP01004L Size: Large In distribution
SP234022 Outer Diameter 4 mm In distribution
SP234035 Length 35 mm In distribution
SP02001R Extra Small, Right In distribution
SP235520 Outer Diameter 5.5 mm In distribution
SP01003L Left In distribution
SP234020 Length 20 mm In distribution
SP224055 Length 55 mm In distribution
SP235560 Outer Diameter 5.5 mm In distribution
SP01004R Right In distribution
SP225560 Length 60 mm In distribution
SP235535 Length 35 mm In distribution
SP234032 Outer Diameter 4 mm In distribution
SP224050 Outer Diameter 4 mm In distribution
SP234034 Outer Diameter 4 mm In distribution
SP235526 Outer Diameter 5.5 mm In distribution
SP225550 Outer Diameter 5.5 mm In distribution
SP225535 Length 35 mm In distribution
SP234045 Outer Diameter 4 mm In distribution
SP224020 Length 20 mm In distribution
SP224026 Locking In distribution
SP235522 Outer Diameter 5.5 mm In distribution
SP02003R Size: Medium In distribution
SP224018 Locking In distribution
SP224022 Outer Diameter 4 mm In distribution
SP224028 Length 28 mm In distribution
SP234030 Length 30 mm In distribution
SP02002R Size: Small In distribution
SP234055 Outer Diameter 4 mm In distribution
SP235538 Outer Diameter 5.5 mm In distribution
SP225522 Length 22 mm In distribution
SP235516 Length 16 mm In distribution
SP225532 Locking In distribution
SP224030 Length 30 mm In distribution
SP224035 Length 35 mm In distribution
SP235518 Outer Diameter 5.5 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pectus System Biomet Microfixation 4,662
Arthrex® Arthrex, Inc. 3,031
Evos Smith & Nephew, Inc. 2,235
Peri-Loc Smith & Nephew, Inc. 2,196
OsteoMed Osteomed 1,961
VariAx Stryker GmbH 1,934
Aptus Medartis Inc. 1,688
TC-100 Smith & Nephew, Inc. 1,639
Plate, Fixation, Bone Synthes Gmbh 1,613
Anthem Globus Medical, Inc. 1,551
Acumed Acumed LLC 1,360
Signex Osteonic Co., Ltd. 1,310

Showing 12 of 3,530. All products under Plate, Fixation, Bone

Recalls

40 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
2023-04-10 Class II Employee error Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts. 50 units
2023-04-10 Class II Employee error Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts. 41 units
2023-02-02 Class II Employee error Stryker has identified an issue that impacts two specific lots of CLAW” II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in packages. Packaging for 402S0425 incorrectly contai 10 units
2023-02-02 Class II Employee error Stryker has identified an issue that impacts two specific lots of CLAW” II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in packages. Packaging for 402S0425 incorrectly contai 4 units
2022-02-15 Class II Process control An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw. 1 package 2022-10-05
2022-02-09 Class II Packaging process control Product was labelled with the incorrect manufacturing and distribution dates. 12 units 2024-01-25
2021-12-03 Class II Under Investigation by firm Incorrect product is contained in the packaging. 22 units
2021-12-03 Class II Under Investigation by firm The incorrect product is contained in the packaging. 23 units
2021-12-03 Class II Under Investigation by firm The incorrect product is contained in the packaging. 250 units
2016-11-08 Class II Process control The firm discovered a lack of adequate documentation confirming sterility on certain products. 30 units 2020-11-03
2016-11-08 Class II Process control The firm discovered a lack of adequate documentation confirming sterility on certain products. 42 units 2020-11-03
2015-07-21 Class II Employee error These screws have a potential of passing through the plate in the case when torque is applied in excessive amounts, which may result in intraoperative malfunction. 5687 units 2018-08-01
2015-07-21 Class II Employee error These screws have a potential of passing through the plate in the case when torque is applied in excessive amounts, which may result in intraoperative malfunction. 107 units 2018-08-01
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 167 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 100 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 233 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction. 52 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction. 92 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 142 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 242 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 270 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 128 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 138 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 102 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 372 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction. 51 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction. 151 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 308 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 172 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 148 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 102 units 2018-08-05
2015-03-06 Class II Nonconforming Material/Component The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction 301 units 2018-08-05
2014-07-30 Class II Device Design Plates manufactured from an incorrect raw material. 0 2018-06-15
2014-07-30 Class II Device Design Plates manufactured from an incorrect raw material. 50 units 2018-06-15
2014-07-30 Class II Device Design Plates manufactured from an incorrect raw material. 1127 units 2018-06-15
2014-07-30 Class II Device Design Plates manufactured from an incorrect raw material. 400 units 2018-06-15
2014-07-30 Class II Device Design Plates manufactured from an incorrect raw material. 9 units 2018-06-15
2014-07-30 Class II Device Design Plates manufactured from an incorrect raw material. 178 units 2018-06-15
2014-07-30 Class II Device Design Plates manufactured from an incorrect raw material. 18 units 2018-06-15
2014-07-30 Class II Device Design Plates manufactured from an incorrect raw material. 66 units 2018-06-15

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