Profix

Profix Flexcr Insert Size 3 14MM Right

Registry build 21.09.26
12manufacturers in China registered for this device type
49catalogue numbers in this listing
11510(k) clearances naming this product code
4recalls on this code

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 Profix
Listed by Smith & Nephew, Inc., 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
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K030623
Record published 2015-08-30
Record revised 2023-09-07 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Distribution end date 2016-06-30

Catalogue Numbers

Catalogue numbers for Profix
Catalogue number Size Status
71503170 Withdrawn
71505240 Withdrawn
71503140 Withdrawn
71505130 Withdrawn
71505120 Withdrawn
71505170 Withdrawn
71507633 Withdrawn
71507563 Withdrawn
71507623 Withdrawn
71503110 Withdrawn
71503220 Withdrawn
71507651 Withdrawn
71505270 Withdrawn
71505260 Withdrawn
71507653 Withdrawn
71507622 Withdrawn
71505250 Withdrawn
71507661 Withdrawn
71507553 Withdrawn
71507631 Withdrawn
71503150 Withdrawn
71505220 Withdrawn
71503260 Withdrawn
71507611 Withdrawn
71503270 Withdrawn
71507511 Withdrawn
71505160 Withdrawn
71505210 Withdrawn
71503250 Withdrawn
71507514 Withdrawn
71503230 Withdrawn
71505150 Withdrawn
71505230 Withdrawn
71503130 Withdrawn
71503160 Withdrawn
71505110 Withdrawn
71507512 Withdrawn
71507561 Withdrawn
71507634 Withdrawn
71503120 Withdrawn
71504350 Withdrawn
71507554 Withdrawn
71507632 Withdrawn
71503240 Withdrawn
71507652 Withdrawn
71505140 Withdrawn
71507522 Withdrawn
71507644 Withdrawn
71507551 Withdrawn

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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K211221 2021-10-01
K211246 2021-05-24
K210566 2021-03-25
K121393 2012-08-07
K100897 2010-05-13
K091543 2009-12-21
K073325 2007-12-20
K071790 2007-08-17
K032683 2003-10-15
K030612 2003-05-27
K030623 2003-05-22

Recalls

4 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
2019-12-16 Class II Process change control Multiple lots of LEGION AP Femoral Cutting Blocks were manufactured with an oversize green plunger hole and therefore do not meet their design specifications. 59 units
2018-09-18 Class II Process control One lot of the Legion AP femoral cutting block, size 6, was manufactured with an oversized spring. 6 units 2019-05-08
2018-05-04 Class II Error in labeling One lot of GENESIS II 13 mm tibial punches are 2 mm smaller than specification. 5 units 2019-02-22
2018-04-09 Class II Process control A single lot of GENESIS II FEMORAL FIVE DEGREE VALGUS BUSHING due to a laser mark labeling error. The left valgus bushing was incorrectly laser marked as right and vice versa. 18 units 2019-02-22

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