Velora Acetabular System Instrumentation

Impactor Cup, Straight, Anti-Rotation, Long Threaded Rod

Registry build 21.09.26
14manufacturers in China registered for this device type
106catalogue numbers in this listing
1510(k) clearance

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 Velora Acetabular System Instrumentation
Listed by restor3d, 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 Complaint-file establishment, Manufacturer
510(k) K252067
Record published 2025-12-12

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
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date, serial number

Catalogue Numbers

Catalogue numbers for Velora Acetabular System Instrumentation
Catalogue number Size Status
5900-RF66 In distribution
6902-K040 In distribution
6901-E036 In distribution
5900-RF37 In distribution
6902-J036 In distribution
5900-RF64 In distribution
5900-RF44 In distribution
6900-B032 In distribution
6902-K036 In distribution
5900-RF58 In distribution
6902-C036 In distribution
6902-B032 In distribution
6902-J040 In distribution
6900-J040 In distribution
6901-C036 In distribution
5900-RF60 In distribution
5900-RF70 In distribution
6900-D036 In distribution
6900-F040 In distribution
6900-G036 In distribution
5900-RF57 In distribution
6901-K040 In distribution
5900-RF68 In distribution
6900-K040 In distribution
6900-J036 In distribution
5900-0008 In distribution
6901-G040 In distribution
5900-RF54 In distribution
6903-A028 In distribution
6903-F036 In distribution
6902-A028 In distribution
5900-RF59 In distribution
6901-D036 In distribution
5900-RF61 In distribution
6903-E040 In distribution
5900-RF36 In distribution
6900-E040 In distribution
5900-0006 In distribution
5900-9002 In distribution
6902-E036 In distribution
5900-RF63 In distribution
5900-RF62 In distribution
6901-K036 In distribution
6903-C036 In distribution
5900-RF67 In distribution
5900-RF55 In distribution
6903-G036 In distribution
6901-H040 In distribution
5900-RF39 In distribution
6900-H040 In distribution
6900-K036 In distribution
5900-RF40 In distribution
5900-RF53 In distribution
6900-G040 In distribution
6903-H040 In distribution
5900-RF49 In distribution
6900-E036 In distribution
6901-J036 In distribution
5900-RF69 In distribution
5900-RF45 In distribution
6903-K036 In distribution
6903-K040 In distribution
6903-B032 In distribution
5900-RF52 In distribution
6900-C036 In distribution
6903-J040 In distribution
6901-B032 In distribution
5900-RF41 In distribution
5900-RF47 In distribution
5900-RF72 In distribution
5900-RF46 In distribution
6902-E040 In distribution
5900-9001 In distribution
6901-J040 In distribution
5900-RF65 In distribution
5900-RF50 In distribution
6901-F036 In distribution
6902-D036 In distribution
6902-G040 In distribution
6903-J036 In distribution
5900-0007 In distribution
6901-H036 In distribution
6903-H036 In distribution
5900-RF43 In distribution
6902-H036 In distribution
6900-F036 In distribution
6902-G036 In distribution
6901-G036 In distribution
6903-E036 In distribution
5900-RF38 In distribution
6903-G040 In distribution
6901-A028 In distribution
6901-F040 In distribution
6903-D036 In distribution
6900-A028 In distribution
5900-RF51 In distribution
6902-F036 In distribution
6903-F040 In distribution
6900-H036 In distribution
6902-H040 In distribution
5900-RF42 In distribution
6902-F040 In distribution
5900-RF71 In distribution
6901-E040 In distribution
5900-RF48 In distribution
5900-RF56 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
K252067 2025-12-05

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