Arcos® One-Piece Revision System

16 catalogue numbers from 110024876, listed by Biomet Orthopedics, United States, under Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
16catalogue numbers in this listing

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (2), Zhejiang (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OQI
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
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

Record

Regulatory record for Arcos® One-Piece Revision System
Listed by Biomet Orthopedics, United States
FDA product code OQI
Device type Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented
Device class Class 2
Regulation 21 CFR 888.3353
510(k) K151603
Record published 2022-04-23
Record revised 2025-05-30 (version 5)

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

Catalogue Numbers

Catalogue numbers for Arcos® One-Piece Revision System
Catalogue number Size Status
110024876 Sizes 9.5 – 14 In distribution
110024880 Sizes 19 – 26 In distribution
11-304412 12 MM 210 MM TYPE 1 TAPER In distribution
11-303422 22 MM 210 MM TYPE 1 TAPER In distribution
110024852 20 mm X 210 mm In distribution
11-303016 16 MM 175 MM TYPE 1 TAPER In distribution
11-303400 9.5 MM 210 MM TYPE 1 TAPER In distribution
11-303021 21 MM 175 MM TYPE 1 TAPER In distribution
11-304117 17 MM 210 MM TYPE 1 TAPER In distribution
11-303421 21 MM 210 MM TYPE 1 TAPER In distribution
110024879 In distribution
110024852 20MM X 210MM In distribution
110024833 18 mm X 175 mm In distribution
11-303017 17 MM 175 MM TYPE 1 TAPER In distribution
11-304022 22 MM 175 MM TYPE 1 TAPER In distribution
11-304015 15 MM 175 MM TYPE 1 TAPER In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Kyocera Medical Technologies, Inc. Kyocera Medical Technologies, Inc. 260
Epore® XO implantcast GmbH 64
G7® Biomet Orthopedics 50
InSitu Hip System Nextstep Arthropedix 50
G7 Acetabular Liner Biomet Orthopedics 47
Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented implantcast GmbH 40
Novation Exactech, Inc. 37
Trinity Acetabular Hip System with ECiMa Liners Corin Limited 28
Procotyl® Prime Microport Orthopedics Inc. 25
AcuMatch Exactech, Inc. 23
Continuum® Trilogy® Allofit® Zimmer, Inc. 23
G7® Longevity® Zimmer, Inc. 23

Showing 12 of 164. All products under Hip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented

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