Maxim Knee System

92 catalogue numbers from 11-146150, listed by Biomet Orthopedics, United States, under Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer. 12 manufacturers in China are registered for this product code.

Registry build 21.09.26
12manufacturers in China registered for this device type
92catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (3), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MBH
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
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
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34

Record

Regulatory record for Maxim Knee System
Listed by Biomet Orthopedics, United States
FDA product code MBH
Device type Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3565
510(k) K142933
Record published 2015-10-24
Record revised 2025-05-30 (version 5)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Maxim Knee System
Catalogue number Size Status
11-146150 10MM 71/75MM In distribution
11-146722 22MM 59MM In distribution
11-146402 22MM 87/91MM In distribution
11-146136 16MM 63/67MM In distribution
145152 65MM In distribution
145171 60MM In distribution
11-146116 16MM 59MM In distribution
145412 65MM In distribution
11-146158 18MM 71/75MM In distribution
11-146572 12MM 79/83MM In distribution
11-146724 24MM 59MM In distribution
140050 55MM In distribution
11-146172 12MM 79/83MM In distribution
145413 70MM In distribution
140070 55MM In distribution
11-146176 16MM 79/83MM In distribution
11-146570 10MM 79/83MM In distribution
11-146112 12MM 59MM In distribution
11-146770 10MM 79/83MM In distribution
145412 65MM In distribution
11-146524 24MM 59MM In distribution
145172 65MM In distribution
11-146356 16MM 71/75MM In distribution
11-146792 12MM 87/91MM In distribution
11-146370 10MM 79/83MM In distribution
11-146716 16MM 59MM In distribution
11-146518 18MM 59MM In distribution
11-146382 22MM 79/83MM In distribution
11-146354 14MM 71/75MM In distribution
11-146396 16MM 87/91MM In distribution
11-146330 10MM 63/67MM In distribution
145174 75MM In distribution
11-146334 14MM 63/67MM In distribution
11-146338 18MM 63/67MM In distribution
11-146156 16MM 71/75MM In distribution
140055 80MM In distribution
11-146740 20MM 63/67MM In distribution
145198 55/60 MM In distribution
11-146564 24MM 71/75MM In distribution
11-146594 14MM 87/91MM In distribution
145411 60MM In distribution
145173 70MM In distribution
11-146510 10MM 59MM In distribution
11-146736 16MM 63/67MM In distribution
11-146762 22MM 71/75MM In distribution
11-146400 20MM 87/91MM In distribution
11-146362 22MM 71/75MM In distribution
11-146342 22MM 63/67MM In distribution
11-146538 18MM 63/67MM In distribution
11-146358 18MM 71/75MM In distribution
11-146800 20MM 87/91MM In distribution
11-146398 18MM 87/91MM In distribution
11-146778 18MM 79/83MM In distribution
140054 75MM In distribution
145414 75MM In distribution
145172 65MM In distribution
11-146404 24MM 87/91MM In distribution
11-146110 10MM 59MM In distribution
11-146794 14MM 87/91MM In distribution
11-146714 14MM 59MM In distribution
11-146604 24MM 87/91MM In distribution
140050 55MM In distribution
11-146174 14MM 79/83MM In distribution
145171 60MM In distribution
11-146514 14MM 59MM In distribution
11-146536 16MM 63/67MM In distribution
11-146752 12MM 71/75MM In distribution
11-146118 18MM 59MM In distribution
145151 60MM In distribution
11-146578 18MM 79/83MM In distribution
11-146802 22MM 87/91MM In distribution
145413 70MM In distribution
145430 55MM In distribution
11-146576 16MM 79/83MM In distribution
11-146734 14MM 63/67MM In distribution
11-146738 18MM 63/67MM In distribution
140070 55MM In distribution
11-146554 14MM 71/75MM In distribution
145433 70MM In distribution
140073 70MM In distribution
145434 75MM In distribution
11-146316 16MM 59MM In distribution
145175 80MM In distribution
11-146376 16MM 79/83MM In distribution
11-146758 18MM 71/75MM In distribution
140054 75MM In distribution
145152 65MM In distribution
145153 70MM In distribution
11-146732 12MM 63/67MM In distribution
11-146352 12MM 71/75MM In distribution
140053 70MM In distribution
11-146322 22MM 59MM In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prophecy Microport Orthopedics Inc. 4,272
Triathlon Howmedica Osteonics Corp 712
Instrument Howmedica Osteonics Corp 709
Persona® Vivacit-E® Zimmer, Inc. 499
Arthrex® Arthrex, Inc. 494
Persona® Zimmer, Inc. 441
Legion Smith & Nephew, Inc. 397
U2 Total Knee System United Orthopedic Corp. 286
Attune Depuy (Ireland) 234
DJO Surgical Encore Medical, L.P. 191
Vanguard XP Instrumentation Biomet Orthopedics 150
Truliant® Exactech, Inc. 142

Showing 12 of 948. All products under Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

Recalls Naming This Product

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

Recalls naming the identifiers of Maxim Knee System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet, Inc. 510(k) number 2018-12-21 Class II Under Investigation by firm Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label. 90 units 2020-05-13
Biomet, Inc. 510(k) number 2018-05-24 Class II Under Investigation by firm Two lots of tibial bearings were commingled. There is a possibility that a 14mm tibial bearing is packaged in a box labeled as 12 mm tibial bearing and vice versa. This may lead to extension of surgery to find another implant. 48 2020-04-07
Biomet, Inc. 510(k) number 2018-05-18 Class II Under Investigation by firm One lot of 75mm tibial tray is potentially etched and labeled as a 79 mm tibial tray. This may lead to delay in surgery, or immediate revision surgery to remove an incorrectly sized tibial component after it has been cemented. 16 2020-03-31
Biomet, Inc. 510(k) number 2018-05-11 Class II Under Investigation by firm The label master file was errantly set up as a 63/37mm instead of a 63/67mm. There is no 63/37 size offered, and the product is laser marked with the correct size. 169 2019-11-21
Biomet, Inc. 510(k) number 2016-12-15 Class II Material/Component Contamination Zimmer Biomet is conducting a medical device recall for ARCOS & TPRLC broaches and rasps due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product c 26 2018-06-29
Biomet, Inc. 510(k) number 2015-04-16 Class III Labeling mix-ups Biomet hip joint, knee joint and shoulder joint replacement components device labeling contains incorrect GTIN (Global Trade Identification Number) codes. 1315 2016-05-16
Biomet, Inc. 510(k) number 2011-03-03 Not classified Packaging process control The firm is recalling the product due to the product’s packaging being labeled “I-Beam 75mm. Tibial Plate”, but the package actually contains the “Interlok 67mm. CR Tibial Plate”. 8 2011-07-27
Biomet, Inc. 510(k) number 2007-12-12 Not classified Packaging process control Mislabeled as to size: Package labeled as containing a 67 mm tray actually contains a 75 mm tray and vice versa. 8 2008-06-11
Biomet, Inc. 510(k) number 2007-12-12 Not classified Packaging process control Mislabeled as to size: Package labeled as containing a 67 mm tray actually contains a 75 mm tray and vice versa. 8 2008-06-11
Biomet, Inc. 510(k) number 2007-09-18 Not classified Labeling mix-ups Mislabeled as to size: the package actaully contained a 71 mm tray. 7 2008-06-04

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