Anatomical Shoulder™

Anatomical Reamer FOR Humeral Stem 10.5

Registry build 21.09.26
9manufacturers in China registered for this device type
166catalogue numbers in this listing
7510(k) clearances naming this product code
20recalls on this code

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (3), Zhejiang (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWS
Manufacturer City Province Registered as Device types
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
Stryker Trauson (Changzhou) Medical Technology Co., Ltd. Changzhou Jiangsu Contract manufacturer 3
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
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34

Record

Regulatory record for Anatomical Shoulder™
Listed by Zimmer, Inc., United States
FDA product code KWS
Device type Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
Device class Class 2
Regulation 21 CFR 888.3660
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k) K142403
Record published 2016-09-24
Record revised 2024-02-19 (version 7)

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
Sizes Outer diameter 5 to 52 mm; length 70 to 200 mm; height 14 to 23 mm
Distribution end date 2017-03-28

Catalogue Numbers

Catalogue numbers for Anatomical Shoulder™
Catalogue number Size Status
01.04558.116 In distribution
01.04201.092 9 In distribution
01.04211.183 Length 120 mm In distribution
01.04215.183 Length 200 mm In distribution
01.04233.140 In distribution
01.04558.120 In distribution
01.04255.000 In distribution
01.04223.018 4.5-18 In distribution
01.04558.118 In distribution
01.04223.033 4.5-33 In distribution
01.04207.143 Ø14-110 In distribution
01.04237.146 In distribution
01.04227.528 Ø52 r=28.5mm In distribution
01.04207.132 Length 130 mm In distribution
01.04223.110 +10° In distribution
01.04212.460 Height 16 mm In distribution
01.04239.600 In distribution
01.04237.126 In distribution
01.04237.125 In distribution
01.04558.111 In distribution
01.04558.117 In distribution
01.04236.534 In distribution
01.04558.300 In distribution
01.04227.364 Ø36 r=19.8mm In distribution
01.04239.610 In distribution
01.04217.112 Length 200 mm In distribution
01.04239.520 In distribution
01.04212.480 Height 17 mm In distribution
01.04236.937 In distribution
01.04558.302 In distribution
01.04239.710 In distribution
01.04214.375 M In distribution
01.04235.181 In distribution
01.04227.404 Ø40 r=22.8mm In distribution
01.04237.135 In distribution
01.04558.115 In distribution
01.04201.072 7 In distribution
01.04207.102 Outer Diameter 10 mm In distribution
01.04223.400 40-0 In distribution
01.04558.104 In distribution
01.04237.445 In distribution
01.04558.126 In distribution
01.04227.403 Ø40 r=22.8mm In distribution
01.04223.100 0° In distribution
01.04233.120 In distribution
01.04237.145 In distribution
01.04232.105 In distribution
01.04558.128 In distribution
01.04227.448 Ø44 r=24.3mm In distribution
01.04237.480 In distribution
01.04239.660 In distribution
01.04237.085 In distribution
01.04558.306 In distribution
01.04207.074 Ø7-110 In distribution
01.04558.121 In distribution
01.04239.234 S In distribution
01.04558.112 In distribution
01.04558.127 In distribution
01.04239.730 In distribution
01.04239.135 In distribution
01.04558.014 In distribution
01.04215.073 Length 90 mm In distribution
01.04211.063 Length 70 mm In distribution
01.04236.540 In distribution
01.04558.102 In distribution
01.04201.053 Length 70 mm In distribution
01.04237.405 In distribution
01.04230.801 In distribution
01.04558.310 In distribution
01.04558.101 In distribution
01.04207.153 Ø15-130 In distribution
01.04558.114 In distribution
01.04237.155 In distribution
01.04237.400 In distribution
01.04217.113 Ø11-180 In distribution
01.04239.250 In distribution
01.04239.130 In distribution
01.04239.810 In distribution
01.04558.311 In distribution
01.04233.070 In distribution
01.04211.123 Length 100 mm In distribution
01.04207.084 Ø8-110 In distribution
01.04239.160 In distribution
01.04207.082 Length 130 mm In distribution
01.04239.560 In distribution
01.04558.100 In distribution
01.04237.705 In distribution
01.04237.086 In distribution
01.04236.934 In distribution
01.04217.092 Length 200 mm In distribution
01.04223.360 36-0 In distribution
01.04558.107 In distribution
01.04237.075 In distribution
01.04239.720 In distribution
01.04558.105 In distribution
01.04237.095 In distribution
01.04223.027 4.5-27 In distribution
01.04237.105 In distribution
01.04239.020 In distribution
01.04223.200 In distribution
01.04558.119 In distribution
01.04215.092 9 In distribution
01.04558.301 In distribution
01.04558.123 In distribution
01.04233.000 In distribution
01.04212.500 Outer Diameter 50 mm In distribution
01.04214.405 L In distribution
01.04558.108 In distribution
01.04236.940 In distribution
01.04237.485 In distribution
01.04236.537 In distribution
01.04215.142 14 In distribution
01.04201.163 Ø16-120 In distribution
01.04237.106 In distribution
01.04201.103 Outer Diameter 10.5 mm In distribution
01.04215.163 Outer Diameter 16 mm In distribution
01.04227.480 Left In distribution
01.04207.113 Ø11-110 In distribution
01.04223.120 +20° In distribution
01.04558.125 In distribution
01.04237.700 In distribution
01.04558.308 In distribution
01.04207.122 Length 130 mm In distribution
01.04215.103 Length 200 mm In distribution
01.04558.307 In distribution
01.04207.112 Length 130 mm In distribution
01.04558.106 In distribution
01.04201.122 12 In distribution
01.04223.111 -10° In distribution
01.04558.110 In distribution
01.04239.530 In distribution
01.04233.090 In distribution
01.04207.133 Ø13-110 In distribution
01.04223.403 40-3 In distribution
01.04558.309 In distribution
01.04230.031 In distribution
01.04212.400 Outer Diameter 40 mm In distribution
01.04211.053 Ø5-70 In distribution
01.04201.102 10.5 In distribution
01.04237.065 In distribution
01.04239.400 In distribution
01.04237.500 In distribution
01.04213.480 Height 20 mm In distribution
01.04239.140 In distribution
01.04558.113 In distribution
01.04558.305 In distribution
01.04213.500 Height 21 mm In distribution
01.04217.133 Ø13-180 In distribution
01.04558.124 In distribution
01.04239.311 In distribution
01.04237.115 In distribution
01.04213.520 Outer Diameter 52 mm In distribution
01.04207.183 Ø18-130 In distribution
01.04223.042 4.5-42 In distribution
01.04211.093 Outer Diameter 9 mm In distribution
01.04233.002 In distribution
01.04558.122 In distribution
01.04237.440 In distribution
01.04214.345 S In distribution
01.04215.143 Ø14-200 In distribution
01.04233.105 In distribution
01.04237.706 In distribution
01.04227.400 Outer Diameter 40 mm In distribution
01.04237.066 In distribution
01.04223.121 -20° In distribution
01.04215.072 7 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Equinoxe Exactech, Inc. 442
Reunion Stryker GmbH 321
DJO Surgical Encore Medical, L.P. 266
SMR Shoulder Limacorporate 209
Tornier Flex Shoulder System Tornier Inc. 187
Arthrex® Arthrex, Inc. 154
Comprehensive Shoulder System Biomet Orthopedics 111
Flex Shoulder System Tornier Inc. 109
Aequalis™ PerFORM+ Tornier Inc. 108
Aequalis™ Ascend™ Flex Tornier Inc. 102
Anatomic Shoulder Prosthesis Medacta International SA 90
Cofield Smith & Nephew, Inc. 76

Showing 12 of 326. All products under Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K193180 2020-02-24
K191814 2019-10-23
K160085 2016-03-08
K142403 2014-11-24
K062029 2006-10-31
K051623 2005-07-19
K870262 1987-04-03

Recalls Naming This Product

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

Recalls naming the identifiers of Anatomical Shoulder™
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Zimmer, Inc. 510(k) number 2016-05-17 Class II Device Design In some cases it has been difficult or not possible to disassemble the adjusted Dome Centric from the AS Humeral Rasp after initial positioning of the AS Humeral Trial Head which resulted in the whole construct of the Dome Centric with the 177 2016-10-31
Zimmer, Inc. 510(k) number 2012-09-04 Class II Error in labeling Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient 260 2014-04-16
Zimmer, Inc. 510(k) number 2012-09-04 Class II Error in labeling Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switzerland, after receiving four complaints of a discrepancy between product patient 139 2014-04-16
Zimmer, Inc. 510(k) number 2012-09-04 Class II Error in labeling Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient 224 2014-04-16
Zimmer, Inc. 510(k) number 2012-09-04 Class II Error in labeling Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient 45 USA 2014-04-16
Zimmer, Inc. 510(k) number 2012-09-04 Class II Error in labeling Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient 54 2014-04-16
Zimmer, Inc. 510(k) number 2012-09-04 Class II Error in labeling Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switzerland, after receiving four complaints of a discrepancy between product patient 26 2014-04-16
Zimmer, Inc. 510(k) number 2012-05-12 Class II Mixed-up of materials/components Bigliani/Flatow The Complete Shoulder Solution Trabecular Metal Glenoid Instrument Drill with Stop, 6 mm. Catalog number 47-4301-031-00 was actually packaged and labeled as catalog number 47-4307-031-00, lot 62071190. 87 units 2013-09-12

Recalls

4 of these are 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
2012-09-04 Class II Error in labeling Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switzerland, after receiving four complaints of a discrepancy between product patient 228 2014-04-16
2012-09-04 Class II Error in labeling Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient 66 2014-04-16
2012-09-04 Class II Error in labeling Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient 164 in USA 2014-04-16
2012-09-04 Class II Error in labeling Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient 74 2014-04-16
2007-06-25 Not classified Other The package actually contains a knee patellar implant. 10 2007-12-05
2005-08-23 Not classified Other The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. 2005-12-08
2005-08-23 Not classified Other The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. 2005-12-08
2005-08-23 Not classified Other The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. 2005-12-08
2005-08-23 Not classified Other The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. 2005-12-08
2005-08-23 Not classified Other The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. 2005-12-08
2005-08-23 Not classified Other The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. 2005-12-08
2005-08-23 Not classified Other The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. 2005-12-08
2005-08-23 Not classified Other The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. 2005-12-08

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