Corail

Corail HIP System Cementless Femoral Stem HA Coated Revision 12/14 AMT 135 Degrees High Offset Collar Size 14

Registry build 21.09.26
15manufacturers in China registered for this device type
35catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (8), 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 LZO
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
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
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
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing 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 15. All 15 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

Record

Regulatory record for Corail
Listed by Depuy (Ireland), Ireland
FDA product code LZO
Device type Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Device class Class 2
Regulation 21 CFR 888.3353
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K042992
Record published 2015-09-24
Record revised 2026-01-16 (version 14)

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
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Corail
Catalogue number Size Status
L98014 In distribution
3L92508 In distribution
L98114 In distribution
L98015 In distribution
L20309 In distribution
L20312 In distribution
3L92510 In distribution
3L92520 In distribution
L98012 In distribution
3L93718 In distribution
3L92503 In distribution
L98020 In distribution
L971112 In distribution
3L92512 In distribution
L20106 In distribution
L20320 In distribution
3L92521 In distribution
L971120 In distribution
L981208 In distribution
3L93710 In distribution
L98013 In distribution
L971118 In distribution
L20315 In distribution
L20318 In distribution
3L92502 In distribution
L98116 In distribution
L98118 In distribution
3L92507 In distribution
3L93712 In distribution
3L93709 In distribution
L98010 In distribution
L971311 In distribution
L981309 In distribution
L20310 In distribution
3L93714 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Libertas Maxx Orthopedics Inc. 1,832
Redapt Smith & Nephew, Inc. 326
Bencox Hip System Corentec Co., Ltd. 295
M-Vizion Femoral Revision System Medacta International SA 289
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Zimmer, Inc. 280
Profemur® Microport Orthopedics Inc. 229
DJO Surgical Encore Medical, L.P. 162
Instrument Howmedica Osteonics Corp 152
Alteon Exactech, Inc. 151
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Exactech, Inc. 136
Resolve Modular Revision Hip Stem United Orthopedic Corp. 136
Wagner SL Revision® Zimmer, Inc. 133

Showing 12 of 691. All products under Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K190344 2019-11-01
K102080 2010-11-23

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