Echo BI-Metric HIP System

21 catalogue numbers from 192121, listed by Biomet Orthopedics, United States, under Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate. 14 manufacturers in China are registered for this product code.

Registry build 21.09.26
14manufacturers in China registered for this device type
21catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (8), Shanghai (2), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MEH
Manufacturer City Province Registered as Device types
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
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54

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

Record

Regulatory record for Echo BI-Metric HIP System
Listed by Biomet Orthopedics, United States
FDA product code MEH
Device type Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
Device class Class 2
Regulation 21 CFR 888.3353
510(k) K070274
Record published 2015-10-24
Record revised 2025-05-30 (version 4)

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

Catalogue Numbers

Catalogue numbers for Echo BI-Metric HIP System
Catalogue number Size Status
192121 21 SIZE 185 MM TYPE I TAPER In distribution
192511 11 Size 135 mm Type I Taper In distribution
192007 7 Size 115 mm Type I Taper In distribution
192519 19 SIZE 175 MM TYPE I TAPER In distribution
192007 7 SIZE 115 MM TYPE I TAPER In distribution
192111 11 Size 135 mm Type I Taper In distribution
192407 7 SIZE 115 MM TYPE I TAPER In distribution
192011 11 Size 135 mm Type I Taper In distribution
192514 14 SIZE 150 MM TYPE I TAPER In distribution
192013 13 SIZE 145 MM TYPE I TAPER In distribution
192014 14 Size 150 mm Type I Taper In distribution
192012 12 Size 140 mm Type I Taper In distribution
192020 20 Size 180 mm Type I Taper In distribution
192420 20 SIZE 180 MM TYPE I TAPER In distribution
192410 10 Size 130 mm Type I Taper In distribution
192409 9 SIZE 125 MM TYPE I TAPER In distribution
192412 12 SIZE 140 MM TYPE I TAPER In distribution
192018 18 SIZE 170 MM TYPE I TAPER In distribution
192510 10 SIZE 130 MM TYPE I TAPER In distribution
192017 17 SIZE 165 MM TYPE I TAPER In distribution
192512 12 SIZE 140 MM TYPE I TAPER In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Alteon Exactech, Inc. 326
Novation Exactech, Inc. 317
Pinnacle Depuy Orthopaedics, Inc. 305
SP-CL Hip Stem Waldemar Link GmbH & Co. KG 219
Emperion Smith & Nephew, Inc. 201
MobileLink Acetabular Cup System Waldemar Link GmbH & Co. KG 154
Instrument Howmedica Osteonics Corp 145
Restoration Howmedica Osteonics Corp 144
Mfinity Femoral System Medacta International SA 138
Echelon Smith & Nephew, Inc. 134
Trinity Acetabular Hip System Corin Limited 128
Redapt Smith & Nephew, Inc. 127

Showing 12 of 805. All products under Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K021403 2002-05-31
K020963 2002-04-16

Recalls Naming This Product

3 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Echo BI-Metric HIP System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet, Inc. 510(k) number 2018-06-08 Class II Process control Two lots of the Echo BI-Metric Hip Stem and ARCOS Modular Revision Hip Stem may have been comingled. Potential health consequences include extension of surgery time to find a replacement component. 12 2020-04-14
Biomet, Inc. 510(k) number 2017-06-05 Class II Labeling False and Misleading Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and actual product are correctly identified but the internal patient label could be incorrect. 2018-03-06
Biomet, Inc. 510(k) number 2012-11-06 Class II Labeling Change Control It was reported that the surgeon noticed that the Echo 11mm hip stem had an etching indicating it was 13mm stem. 4 2013-08-28

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