Profemur®

Profemur® Renaissance® Classic STD Flare SZ 16 V8DG Long Neck

Registry build 21.09.26
14manufacturers in China registered for this device type
100catalogue numbers in this listing
6510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (3), Zhejiang (2). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LPH
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
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Xian Airfoil Technology Co., Ltd. Xian Shaanxi Contract manufacturer 8
Lincotek (Wuxi) Co., Ltd. Wuxi Jiangsu Contract manufacturer 7
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

Showing 12 of 14. All 14 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Record

Regulatory record for Profemur®
Listed by Microport Orthopedics Inc., United States
FDA product code LPH
Device type Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Device class Class 2
Regulation 21 CFR 888.3358
Establishment Contract manufacturer, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K141235
Record published 2015-10-20
Record revised 2018-07-06 (version 3)

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, manufacturing date
Sizes Length 110 to 139 mm

Catalogue Numbers

Catalogue numbers for Profemur®
Catalogue number Size Status
PHAPS246 In distribution
PLLSS013 In distribution
PHAC1204 In distribution
PHAPS244 In distribution
PHA0E242 In distribution
PHA0S248 In distribution
PLLES016 In distribution
PYRD0008 In distribution
PHAPE248 In distribution
PHAPS248 In distribution
PHA00238 Length 121 mm In distribution
PGHCCLE6 In distribution
PYRD0001 In distribution
PHA0S240 In distribution
PHAPS242 In distribution
PHA0S246 In distribution
PPW38073 In distribution
PHAPE240 In distribution
PHAC1212 In distribution
PRGLDC12 In distribution
PLLSR015 In distribution
PHA00232 Length 110 mm In distribution
PLLER011 In distribution
PLLER015 In distribution
PHA00236 Length 118 mm In distribution
PGHCCLE1 In distribution
PHA00248 Length 139 mm In distribution
PYRD0005 In distribution
PHAPE244 In distribution
PHA00244 Length 132 mm In distribution
PLLSS018 In distribution
PGHCCLS1 In distribution
PHA0E248 In distribution
PRGLDC08 In distribution
PHA0E234 In distribution
PHAPS232 In distribution
PHA0S236 In distribution
PHA0E244 In distribution
PLLSR011 In distribution
PHAPS234 In distribution
PHAPE238 In distribution
PHA0S242 In distribution
PHA0E232 In distribution
PYRD0003 In distribution
PHA0S232 In distribution
PHAPE236 In distribution
PLLER011 In distribution
PLLES010 In distribution
PGHCCLS8 In distribution
PHA00242 Length 128 mm In distribution
PHAC1244 In distribution
PHAPS238 In distribution
PHA00234 Length 114 mm In distribution
PHAPE232 In distribution
PLLES014 In distribution
PYRD0006 In distribution
PLLES018 In distribution
PHAPE242 In distribution
PYRD0002 In distribution
PGHCCLS2 In distribution
PHA0E246 In distribution
PGHCCE10 In distribution
PHAPE246 In distribution
PHA0S238 In distribution
PLLSR012 In distribution
PYRD0009 In distribution
PHAPS240 In distribution
PLLES012 In distribution
PLLES012 In distribution
PRGLCM12 In distribution
PRGLDC04 In distribution
PHAPE234 In distribution
PLLSS016 In distribution
PYRD0007 In distribution
PGHCCLE5 In distribution
PHA00240 Length 125 mm In distribution
PLLES016 In distribution
PLLSS012 In distribution
PLLSR015 In distribution
PHA0E240 In distribution
PLLSS012 In distribution
PLLSR013 In distribution
PRGLCM04 In distribution
PHA0E238 In distribution
PHAPS236 In distribution
PHAC1204 In distribution
PRGLCM08 In distribution
PLLSS014 In distribution
PHA00246 Length 136 mm In distribution
PLLES014 In distribution
PHA0S234 In distribution
PHA0S244 In distribution
PYRD0004 In distribution
PHA0E236 In distribution
PLLSS010 In distribution
PLLES010 In distribution
PLLER013 In distribution
PHAC1224 In distribution
PHAC1254 In distribution
PHAC1214 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Initia Total Hip System Kyocera Medical Technologies, Inc. 1,000
DJO Surgical Encore Medical, L.P. 624
Pinnacle Depuy Orthopaedics, Inc. 613
Trilogy® Longevity® Zimmer, Inc. 564
Instrument Howmedica Osteonics Corp 369
InSitu Hip System Nextstep Arthropedix 368
Trilogy® Zimmer, Inc. 359
Kyocera Medical Technologies, Inc. Kyocera Medical Technologies, Inc. 298
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented Zimmer, Inc. 286
Bencox Hip System Corentec Co., Ltd. 286
OrthoMedFlex Orthomedflex LLC 257
Sterizo Total Hip System CPM Medical Consultants, LLC. 240

Showing 12 of 792. All products under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K240046 2024-04-18
K200011 2021-10-01
K190123 2019-07-15
K180798 2018-07-09
K170444 2017-06-26
K142119 2015-02-27

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.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P880025 1991-12-04 AML(R) POROCOAT(R) ACETABULAR CUP PROSTHESIS Depuy Intl., Ltd.
P880076 1991-06-17 WHITESIDE EPS(TM) FEMORAL HIP PROSTHESIS Dow Corning Wright
P850061 1991-03-08 BIAS(R) FIBER METAL TOTAL HIP SYSTEM Zimmer, Inc.

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