Remedy Spacer

REMEDY® Acetabular Cup 40mm ID/48mm OD

Registry build 21.09.26
10manufacturers in China registered for this device type
11catalogue numbers in this listing
6510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (4), Shanghai (3), Zhejiang (2). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWL
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
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Xian Airfoil Technology Co., Ltd. Xian Shaanxi Contract manufacturer 8
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 Remedy Spacer
Listed by Osteoremedies, LLC, United States
FDA product code KWL
Device type Prosthesis, Hip, Hemi-, Femoral, Metal
Device class Class 2
Regulation 21 CFR 888.3360
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K112470
Record published 2016-01-20
Record revised 2018-07-06 (version 3)

Specifications

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

Catalogue Numbers

Catalogue numbers for Remedy Spacer
Catalogue number Size Status
RHLSSM In distribution
RHLSMD In distribution
RHSTSM In distribution
RHACXS In distribution
RHHDXS In distribution
RHHDLG In distribution
RHSTLG In distribution
RHLSLG In distribution
RHSTMD In distribution
RHHDSM In distribution
RHHDMD In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Ustar II Knee System United Orthopedic Corp. 115
Consensus Hip System Shalby Advanced Technologies, Inc. 95
Consensus® Hip System Consensus Orthopedics, Inc. 95
Instrument Howmedica Osteonics Corp 94
UHR Howmedica Osteonics Corp 75
Austin Moore Howmedica Osteonics Corp 67
B-P Total HIP System Endotec, Inc. 66
CS2 Acetabular Cup System Consensus Orthopedics, Inc. 64
DJO Surgical Encore Medical, L.P. 62
Restoration Howmedica Osteonics Corp 56
Optimom Modular Heads Corin Limited 49
Corin Unipolar Modular Head Corin Limited 36

Showing 12 of 167. All products under Prosthesis, Hip, Hemi-, Femoral, Metal

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K262290 2026-07-24
K253675 2025-12-23
K192995 2020-01-10
K191981 2019-08-23
K172906 2018-08-29
K173967 2018-02-22

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