Restoris

Tibial Baseplate Template Std RM/LL Sz8

Registry build 21.09.26
6manufacturers in China registered for this device type
105catalogue numbers in this listing
6510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (2), Jiangsu (2), Shanghai (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HSX
Manufacturer City Province Registered as Device types
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
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74

Record

Regulatory record for Restoris
Listed by Mako Surgical Corp., United States
FDA product code HSX
Device type Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3520
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K082172
Record published 2016-09-24
Record revised 2022-03-22 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Sizes Length 1 in; height 15 mm

Catalogue Numbers

Catalogue numbers for Restoris
Catalogue number Size Status
160117 Side: RIGHT In distribution
180725-4 Thickness: 9.5 Millimeter In distribution
180722-9 Thickness: 14.5 Millimeter In distribution
170703-5 Size: 3 In distribution
180728-5 Size: 8 In distribution
180701-1 Thickness: 8.0 Millimeter In distribution
170701-7 Thickness: 14.0 Millimeter In distribution
170405 Size: 5 In distribution
180707-5 Size: 7 In distribution
170517 Side: Right Medial/Left Lateral In distribution
180507 Side: Left Medial/Right Lateral In distribution
180726-3 Thickness: 8.5 Millimeter In distribution
170708-9 Size: 8 In distribution
180708-3 Thickness: 10.0 Millimeter In distribution
180721-1 Thickness: 6.5 Millimeter In distribution
160104 Side: LEFT In distribution
170407 Size: 7 In distribution
160116 Side: RIGHT In distribution
170713-3 Thickness: 8.5 Millimeter In distribution
180512 Size: 2 In distribution
170602 Side: Left Medial/Right Lateral In distribution
170703-1 Thickness: 8.0 Millimeter In distribution
180606 Side: Left Medial/Right Lateral In distribution
180728-2 Size: 8 In distribution
170707-4 Size: 7 In distribution
180408 Size: 8 In distribution
170707-3 Size: 7 In distribution
170707-6 Thickness: 13.0 Millimeter In distribution
170504 Size: 4 In distribution
160123 Side: Left Medial/Right Lateral In distribution
180723-8 Thickness: 13.5 Millimeter In distribution
180704-1 Size: 4 In distribution
180413 Size: 3 In distribution
170701-5 Thickness: 12.0 Millimeter In distribution
180707-6 Size: 7 In distribution
180722-8 Size: 2 In distribution
170714-2 Thickness: 7.5 Millimeter In distribution
170518 Size: 8 In distribution
180704-5 Thickness: 12.0 Millimeter In distribution
180728-8 Size: 8 In distribution
180406 Side: LEFT In distribution
180723-3 Size: 3 In distribution
160158 Side: Right Medial/Left Lateral In distribution
180614 Size: 4 In distribution
160170 In distribution
170505 Side: Left Medial/Right Lateral In distribution
160131 Side: Right Medial/Left Lateral In distribution
180721-5 Thickness: 10.5 Millimeter In distribution
170320-3 Diameter: 32.0 Millimeter In distribution
180726-4 Size: 6 In distribution
180724-7 Size: 4 In distribution
160108 Side: LEFT In distribution
111541-2 Diameter: 35.0 Millimeter In distribution
180723-4 Size: 3 In distribution
180706-4 Size: 6 In distribution
180728-9 Thickness: 14.5 Millimeter In distribution
180604 Size: 4 In distribution
180727-3 Size: 7 In distribution
180723-6 Thickness: 11.5 Millimeter In distribution
160155 Size: 5 In distribution
170513 Size: 3 In distribution
111541-1 Diameter: 26.0 Millimeter In distribution
170711-1 Thickness: 6.5 Millimeter In distribution
160156 Size: 6 In distribution
180702-6 Size: 2 In distribution
180518 Size: 8 In distribution
180702-1 Size: 2 In distribution
160138 Size: 8 In distribution
170705-9 Size: 5 In distribution
170417 Side: RIGHT In distribution
180724-6 Size: 4 In distribution
180706-7 Size: 6 In distribution
160121 Side: Left Medial/Right Lateral In distribution
170704-5 Thickness: 12.0 Millimeter In distribution
160127 Side: Left Medial/Right Lateral In distribution
180724-1 Thickness: 6.5 Millimeter In distribution
180418 Size: 8 In distribution
160126 Size: 6 In distribution
160103 Size: 3 In distribution
180320-6 Diameter: 41.0 Millimeter In distribution
111540 In distribution
180505 Side: Left Medial/Right Lateral In distribution
180705-1 Size: 5 In distribution
180407 Size: 7 In distribution
180721-9 Size: 1 In distribution
180708-2 Thickness: 9.0 Millimeter In distribution
160135 Size: 5 In distribution
170412 Size: 2 In distribution
120209-5 Length 1.0 in In distribution
180412 Side: RIGHT In distribution
170716-2 Size: 6 In distribution
170320-4 Diameter: 35.0 Millimeter In distribution
180721-8 Size: 1 In distribution
160172 In distribution
180705-4 Size: 5 In distribution
160195 In distribution
180726-5 Size: 6 In distribution
170705-4 Thickness: 11.0 Millimeter In distribution
160134 Size: 4 In distribution
170701-1 Size: 1 In distribution
180403 Side: LEFT In distribution
170701-6 Size: 1 In distribution
180707-1 Thickness: 8.0 Millimeter In distribution
180701-8 Height 15.0 mm In distribution
180728-1 Thickness: 6.5 Millimeter In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Journey Smith & Nephew, Inc. 517
Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer Ortho Development Corp. 303
BKS® Uni Ortho Development Corp. 240
LinkSymphoKnee Waldemar Link GmbH & Co. KG 210
Moto Partial Knee System Medacta International SA 205
Arthrex® Arthrex, Inc. 199
Stride Smith & Nephew, Inc. 190
Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer Zimmer, Inc. 175
ZUK Smith & Nephew, Inc. 161
Tahoe Uni Knee System Shalby Advanced Technologies, Inc. 134
Moto Partial Knee System – Medial Medacta International SA 132
Journey II Smith & Nephew, Inc. 119

Showing 12 of 171. All products under Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K220930 2022-06-02
K082172 2008-11-28
K082081 2008-10-15
K080368 2008-06-20
K073248 2007-12-12
K060017 2006-02-23

Recalls Naming This Product

5 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Restoris
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Howmedica Osteonics Corp 510(k) number 2023-03-10 Class II Process change control Ccertain lots of the Restoris MultiCompartmental Knee (MCK) Tibial Baseplate Trials contain product with incorrect size laser marking 52 units
Howmedica Osteonics Corp 510(k) number 2023-03-10 Class II Process change control Certain lots of the Restoris MultiCompartmental Knee (MCK) Tibial Baseplate Trials contain product with incorrect size laser marking 102 units
Mako Surgical Corp. 510(k) number 2018-01-19 Class II Under Investigation by firm Possible hinge pin disassociation from the Mako Onlay Insert Extractor. 575 units total (400 US, 175 OUS) 2020-09-16
Mako Surgical Corp. 510(k) number 2016-01-15 Class II Unknown/Undetermined by firm Reports where the Mylar/Tyvek pouch for RESTORIS MCK Baseplate in the clamshell packaging configuration exhibited damage, compromising the sterile barrier. 146 2019-08-06
Mako Surgical Corp. 510(k) number 2014-01-09 Class II Error in labeling The product may be mislabeled and could result in the incorrect implant being used. 41 units 2014-08-14

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