Escalade Acetabular System

Dia.6.5x35mm Cancellous Bone Screw Low Profile

Registry build 21.09.26
15manufacturers in China registered for this device type
77catalogue numbers in this listing
6510(k) clearances naming this product code
5recalls on this code

Who Else Makes It

Concentrated in Jiangsu (8), Shanghai (3), Zhejiang (2). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LZO
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
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
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

Showing 12 of 15. All 15 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

Record

Regulatory record for Escalade Acetabular System
Listed by Ortho Development Corp., United States
FDA product code LZO
Device type Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Device class Class 2
Regulation 21 CFR 888.3353
Establishment Specification developer, Complaint-file establishment, Manufacturer, Exporter
510(k) K103384
Record published 2015-08-31
Record revised 2025-02-06 (version 7)

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 6.5 to 70 mm; lumen/inner diameter 22 to 40 mm; length 1 to 60 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Escalade Acetabular System
Catalogue number Size Status
171-2848 Outer Diameter 48 mm In distribution
170-0042 Outer Diameter 42 mm In distribution
171-2844 Length 3 mm In distribution
170-3055 Length 55 mm In distribution
170-0068 Outer Diameter 68 mm In distribution
170-3664 Lumen/Inner Diameter 36 mm In distribution
170-0062 Outer Diameter 62 mm In distribution
170-3030 Length 30 mm In distribution
171-3664 Outer Diameter 64 mm In distribution
171-4056 Length 3 mm In distribution
170-0360 Outer Diameter 60 mm In distribution
170-0046 Outer Diameter 46 mm In distribution
170-2035 Length 35 mm In distribution
170-0162 Outer Diameter 62 mm In distribution
170-0168 Outer Diameter 68 mm In distribution
170-0166 Outer Diameter 66 mm In distribution
170-3045 Length 45 mm In distribution
170-0362 Outer Diameter 62 mm In distribution
170-0070 Outer Diameter 70 mm In distribution
170-0146 Outer Diameter 46 mm In distribution
170-0142 Outer Diameter 42 mm In distribution
170-0164 Outer Diameter 64 mm In distribution
170-2015 Outer Diameter 6.5 mm In distribution
170-0350 Outer Diameter 50 mm In distribution
171-3256 Outer Diameter 56 mm In distribution
170-3254 Lumen/Inner Diameter 32 mm In distribution
171-4058 Lumen/Inner Diameter 40 mm In distribution
170-0054 Outer Diameter 54 mm In distribution
170-0156 Outer Diameter 56 mm In distribution
171-3654 Lumen/Inner Diameter 36 mm In distribution
170-3256 Outer Diameter 56 mm In distribution
170-2060 Outer Diameter 6.5 mm In distribution
170-0150 Outer Diameter 50 mm In distribution
171-2858 Lumen/Inner Diameter 28 mm In distribution
170-0340 Outer Diameter 40 mm In distribution
170-4056 Outer Diameter 56 mm In distribution
170-0352 Outer Diameter 52 mm In distribution
170-2642 Lumen/Inner Diameter 26 mm In distribution
171-2860 Outer Diameter 60 mm In distribution
171-4060 Lumen/Inner Diameter 40 mm In distribution
170-0354 Outer Diameter 54 mm In distribution
170-4062 Lumen/Inner Diameter 40 mm In distribution
171-3248 Outer Diameter 48 mm In distribution
170-0152 Outer Diameter 52 mm In distribution
170-3258 Lumen/Inner Diameter 32 mm In distribution
170-4064 Lumen/Inner Diameter 40 mm In distribution
170-3252 Lumen/Inner Diameter 32 mm In distribution
170-2055 Length 55 mm In distribution
170-3015 Length 15 mm In distribution
170-0048 Outer Diameter 48 mm In distribution
170-0050 Outer Diameter 50 mm In distribution
171-3652 Lumen/Inner Diameter 36 mm In distribution
170-3658 Lumen/Inner Diameter 36 mm In distribution
171-2864 Lumen/Inner Diameter 28 mm In distribution
170-0066 Outer Diameter 66 mm In distribution
171-3250 Length 1 mm In distribution
170-3652 Length 3 mm In distribution
171-3254 Lumen/Inner Diameter 32 mm In distribution
171-2846 Lumen/Inner Diameter 28 mm In distribution
170-3050 Length 50 mm In distribution
170-2644 Lumen/Inner Diameter 26 mm In distribution
170-0040 Outer Diameter 40 mm In distribution
170-3656 Lumen/Inner Diameter 36 mm In distribution
170-0158 Outer Diameter 58 mm In distribution
170-0366 Outer Diameter 66 mm In distribution
170-0348 Outer Diameter 48 mm In distribution
170-2856 Outer Diameter 56 mm In distribution
170-0364 Outer Diameter 64 mm In distribution
170-2858 Outer Diameter 58 mm In distribution
170-0356 Outer Diameter 56 mm In distribution
170-2846 Lumen/Inner Diameter 28 mm In distribution
171-2240 Lumen/Inner Diameter 22 mm In distribution
170-0346 Outer Diameter 46 mm In distribution
171-3260 Outer Diameter 60 mm In distribution
170-3020 Length 20 mm In distribution
170-2025 Length 25 mm In distribution
170-2862 Lumen/Inner Diameter 28 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Libertas Maxx Orthopedics Inc. 1,832
Redapt Smith & Nephew, Inc. 326
Bencox Hip System Corentec Co., Ltd. 295
M-Vizion Femoral Revision System Medacta International SA 289
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Zimmer, Inc. 280
Profemur® Microport Orthopedics Inc. 229
DJO Surgical Encore Medical, L.P. 162
Instrument Howmedica Osteonics Corp 152
Alteon Exactech, Inc. 151
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Exactech, Inc. 136
Resolve Modular Revision Hip Stem United Orthopedic Corp. 136
Wagner SL Revision® Zimmer, Inc. 133

Showing 12 of 691. All products under Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K111936 2011-09-21
K060577 2006-04-28
K053587 2006-03-17
K970675 1997-08-22
K971426 1997-07-09
K971435 1997-07-09

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 Escalade Acetabular System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Ortho Development Corp. 510(k) number 2011-12-19 Not classified Device Design Tip of hex-head screwdriver may break off during use in hip replacement procedure. 37 units 2012-08-27

Recalls

The FDA has not published a severity grade for these. 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
2011-01-11 Not classified Process design Component of total hip arthroplasty may break during surgical procedure. 7 units 2011-11-04
2011-01-11 Not classified Process design Component of total hip arthroplasty may break during surgical procedure. 33 units 2011-11-04
2011-01-11 Not classified Process design Component of total hip arthroplasty may break during surgical procedure. 7 units 2011-11-04
2011-01-11 Not classified Process design Component of total hip arthroplasty may break during surgical procedure. 33 units 2011-11-04

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