Trilogy®

21 catalogue numbers from 65-6200-60-22, listed by Zimmer, Inc., 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
2recalls on this 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 Trilogy®
Listed by Zimmer, Inc., 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
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k) K980711
Record published 2017-12-08
Record revised 2021-07-19 (version 5)

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
Sizes Outer diameter 36 to 80 mm

Catalogue Numbers

Catalogue numbers for Trilogy®
Catalogue number Size Status
65-6200-60-22 Outer Diameter 60 mm In distribution
65-6200-42-21 Outer Diameter 42 mm In distribution
65-6200-64-21 Outer Diameter 64 mm In distribution
65-6200-68-22 Outer Diameter 68 mm In distribution
65-6200-36-20 Outer Diameter 36 mm In distribution
65-6200-56-22 Outer Diameter 56 mm In distribution
65-6200-50-21 Outer Diameter 50 mm In distribution
65-6200-60-21 Outer Diameter 60 mm In distribution
65-6200-66-21 Outer Diameter 66 mm In distribution
65-6200-66-20 Outer Diameter 66 mm In distribution
65-6200-44-21 Outer Diameter 44 mm In distribution
65-6200-62-21 Outer Diameter 62 mm In distribution
65-6200-52-22 Outer Diameter 52 mm In distribution
65-6200-40-21 Outer Diameter 40 mm In distribution
65-6200-72-20 Outer Diameter 72 mm In distribution
65-6200-80-20 Outer Diameter 80 mm In distribution
65-6200-66-22 Outer Diameter 66 mm In distribution
65-6200-48-22 Outer Diameter 48 mm In distribution
65-6200-64-20 Outer Diameter 64 mm In distribution
65-6200-70-20 Outer Diameter 70 mm In distribution
65-6200-58-21 Outer Diameter 58 mm 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
K925607 1993-11-08
K912263 1991-08-29

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Trilogy®
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Zimmer, Inc. 510(k) number 2012-09-14 Class II Process control Some units of Trilogy shells manufactured since March 2009 may be below the lower range of the pore size specification (as low as 28% vs. 30% porosity specification). On 10/31/2012, the firm expanded the recall action to include lots of Uni 275,952 units 2014-06-20

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2014-12-17 Class II Package design/selection Potential compromise of the inner sterile tray. If a compromised tray is detected, a delay in surgery may result. If undetected breach in both the inner and outer trays were to occur, and there is contamination present, a periprosthetic inf 6109 2015-09-23

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