Perfecta

Perfecta® RA Cocr Polished HIP Size 16.5 SLT Taper Collarless

Registry build 21.09.26
13manufacturers in China registered for this device type
30catalogue numbers in this listing
2510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (3), Zhejiang (2). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JDI
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
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
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing 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
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54

Showing 12 of 13. All 13 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Record

Regulatory record for Perfecta
Listed by Microport Orthopedics Inc., United States
FDA product code JDI
Device type Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Device class Class 2
Regulation 21 CFR 888.3350
Establishment Contract manufacturer, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-10-20
Record revised 2018-03-29 (version 2)

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, manufacturing date
Sizes Outer diameter 9 to 15 mm

Catalogue Numbers

Catalogue numbers for Perfecta
Catalogue number Size Status
37561650 In distribution
37931351 In distribution
37881420 Outer Diameter 14.2 mm In distribution
37801500 In distribution
37561050 In distribution
37871420 Outer Diameter 14.2 mm In distribution
37931052 In distribution
37561500 In distribution
37931203 In distribution
37801200 In distribution
37871270 Outer Diameter 12.7 mm In distribution
37881270 Outer Diameter 12.7 mm In distribution
37931352 In distribution
37881350 Outer Diameter 13.5 mm In distribution
37931202 In distribution
37871500 Outer Diameter 15.0 mm In distribution
37561200 In distribution
37880900 Outer Diameter 9.0 mm In distribution
37811800 In distribution
37811200 In distribution
37931051 In distribution
37881050 Outer Diameter 10.5 mm In distribution
37931201 In distribution
37801800 In distribution
37871350 Outer Diameter 13.5 mm In distribution
37881500 Outer Diameter 15.0 mm In distribution
37561800 In distribution
37811500 In distribution
37561350 In distribution
37881200 Outer Diameter 12.0 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented Zimmer, Inc. 836
R3 Smith & Nephew, Inc. 497
UniSyn Hip System Shalby Advanced Technologies, Inc. 247
UniSyn® Hip System Consensus Orthopedics, Inc. 247
Reflection Smith & Nephew, Inc. 170
Instrument Howmedica Osteonics Corp 167
Echelon Smith & Nephew, Inc. 159
B-P Total HIP System Endotec, Inc. 151
ZCA® Zimmer, Inc. 149
Omnifit Howmedica Osteonics Corp 149
Ringloc HIP System Biomet Orthopedics 139
Profemur Microport Orthopedics Inc. 113

Showing 12 of 444. All products under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K213816 2022-01-05
K201519 2020-12-10

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
2022-05-04 Class II Process change control One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body. 8 units 2024-01-16

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