Comprehensive Shoulder System
111 catalogue numbers from 41-405816, listed by Biomet Orthopedics, United States, under Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented. 9 manufacturers in China are registered for this product code.
9manufacturers in China registered for this device type
111catalogue numbers in this listing
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.
| 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
| Listed by | Biomet Orthopedics, United States |
|---|---|
| FDA product code | KWS |
| Device type | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3660 |
| 510(k) | K060692 |
| Record published | 2016-10-25 |
| Record revised | 2025-10-30 (version 8) |
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 |
| Distribution end date | 2016-10-04 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 41-405816 | 16MM | In distribution |
| 113656 | 16 MM 122MM LONG | In distribution |
| 407308 | 8 mm | In distribution |
| 113657 | 17 MM 122MM LONG | In distribution |
| 407331 | 11MM | In distribution |
| 113619 | 19 mm 55mm Long | In distribution |
| 113650 | 10 MM 122MM LONG | In distribution |
| 110017162 | Standard | In distribution |
| 113614 | 14 MM 55MM LONG | In distribution |
| 113044 | 46MM HEAD Ø 21MM HEIGHT 50MM Ø OF CURV | In distribution |
| 113579 | 11MM SLEEVE | In distribution |
| 113638 | 18 MM 83MM LONG | In distribution |
| 407334 | 14MM | In distribution |
| 405307 | 7MM | In distribution |
| 405317 | 17MM | In distribution |
| 41-405815 | 15MM | In distribution |
| 113658 | 18 MM 122MM LONG | In distribution |
| 180565 | 4.75MM Ø 20MM LENGTH 3.5MM HEX | In distribution |
| 407007 | 9 mm | In distribution |
| 41-405812 | 12MM | In distribution |
| 180575 | 4.75MM Ø 35MM LENGTH 3.5MM HEX | In distribution |
| 113580 | 12MM SLEEVE | In distribution |
| 113606 | 6 MM 55MM LONG | In distribution |
| 31-406904 | 4 mm | In distribution |
| 113034 | 42MM HEAD Ø 21MM HEIGHT 43MM Ø OF CURV | In distribution |
| 113628 | 8 MM 83MM LONG | In distribution |
| 113637 | 17 mm 83mm Long | In distribution |
| 113048 | 46MM HEAD Ø 27MM HEIGHT 46MM Ø OF CURV | In distribution |
| 11-113564 | 14 mm 122mm Long | In distribution |
| 407006 | 8MM | In distribution |
| 113136 | 42MM HEAD Ø 24MM HEIGHT 42MM Ø OF CURV | In distribution |
| 110004319 | In distribution | |
| 405316 | 16MM | In distribution |
| 113342 | 46MM HEAD Ø 18MM HEIGHT 53MM Ø OF CURV | In distribution |
| 11-113554 | 4 MM 122MM LONG | In distribution |
| 113057 | 50MM HEAD Ø 27MM HEIGHT 50MM Ø OF CURV | In distribution |
| 407014 | 16 mm | In distribution |
| 41-405810 | 10MM | In distribution |
| 407009 | 11 mm | In distribution |
| TI-113036 | 42MM HEAD Ø 24MM HEIGHT 42MM Ø OF CURV | In distribution |
| 113604 | 4 MM 55MM LONG | In distribution |
| 12-113560 | 10 MM 122MM LONG | In distribution |
| 113630 | 10 mm 83mm Long | In distribution |
| 113616 | 16 mm 55mm Long | In distribution |
| 113618 | 18 MM 55MM LONG | In distribution |
| 407318 | 18 mm | In distribution |
| 118000 | In distribution | |
| 113585 | 17MM SLEEVE | In distribution |
| 407034 | 16 mm / 17 mm | In distribution |
| 113649 | 9 mm 122mm Long | In distribution |
| 41-405809 | 9MM | In distribution |
| 407306 | In distribution | |
| 113582 | 14MM SLEEVE | In distribution |
| 41-405819 | 19MM | In distribution |
| 407325 | 5MM | In distribution |
| 113658 | 18 mm 122mm Long | In distribution |
| TI-113034 | 42MM HEAD Ø 21MM HEIGHT 43MM Ø OF CURV | In distribution |
| 405307 | 7 mm | In distribution |
| 113647 | 7 mm 122mm Long | In distribution |
| 41-405808 | 8MM | In distribution |
| 407348 | In distribution | |
| 407007 | In distribution | |
| 31-406904 | In distribution | |
| 113583 | 15MM SLEEVE | In distribution |
| 113646 | 6 mm 122mm Long | In distribution |
| 407316 | In distribution | |
| 113575 | 7MM SLEEVE | In distribution |
| 407030 | 12 mm / 13 mm | In distribution |
| TI-113022 | 38MM HEAD Ø 19MM HEIGHT 39MM Ø OF CURV | In distribution |
| 41-405813 | 13MM | In distribution |
| 407012 | In distribution | |
| 41-405817 | 17MM | In distribution |
| 407310 | In distribution | |
| 405320 | 20 mm | In distribution |
| 113631 | 11 MM 83MM LONG | In distribution |
| 113655 | 15 MM 122MM LONG | In distribution |
| 113640 | 20 MM 83MM LONG | In distribution |
| 405319 | 19 mm | In distribution |
| 405304 | 4 mm | In distribution |
| 180576 | 4.75MM Ø 40MM LENGTH 3.5MM HEX | In distribution |
| 407011 | 13 mm | In distribution |
| 113627 | 7 MM 83MM LONG | In distribution |
| 407315 | In distribution | |
| 113668 | 8 MM 194 MM | In distribution |
| 113653 | 13 mm 122mm Long | In distribution |
| 113646 | 6 MM 122MM LONG | In distribution |
| 113605 | 5 MM 55MM LONG | In distribution |
| 405311 | 11 mm | In distribution |
| 407305 | 5 mm | In distribution |
| 113063 | 54MM HEAD Ø 21MM HEIGHT 64MM Ø OF CURV | In distribution |
| 405315 | 15MM | In distribution |
| 41-405805 | 5MM | In distribution |
| 407012 | 14 mm | In distribution |
| 113578 | 10MM SLEEVE | In distribution |
| 407352 | In distribution | |
| 113627 | 7 mm 83mm Long | In distribution |
| 113032 | 42MM HEAD Ø 18MM HEIGHT 46MM Ø OF CURV | In distribution |
| 405309 | 9 mm | In distribution |
| 407014 | 16MM | In distribution |
| 110017162 | STANDARD | In distribution |
| 31-406908 | In distribution | |
| 11-113560 | 10 mm 122mm Long | In distribution |
| 113666 | 6 MM 194 MM | In distribution |
| 407310 | 10 mm | In distribution |
| 113644 | 4 MM 122MM LONG | In distribution |
| 113605 | 5 mm 55mm Long | In distribution |
| 405312 | 12 mm | In distribution |
| SSI001964 | Withdrawn | |
| SSI000167 | SM | Withdrawn |
| SSI001765 | MD | Withdrawn |
| SSI001757 | LG | Withdrawn |
Same 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 |
| Anatomical Shoulder™ | Zimmer, Inc. | 166 |
| Arthrex® | Arthrex, Inc. | 154 |
| 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
Recalls Naming This Product
36 recalls name this product by its own identifiers, the UDI on its label or the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Zimmer Orthopedics Manufacturing Limited-Galway | 510(k) number | 2025-03-03 | Class II | Nonconforming Material/Component | Five complaints received where surgeon was unable to remove and/or connect the inserter with the stem during surgery due to excess material remaining within the taper. Issue may lead to clinically significant extension of surgery to find a | 90 US; 136 OUS | |
| Biomet, Inc. | UDI-DI | 2022-01-07 | Class II | Process control | The products in scope underwent an incorrect rework operation for the porous plasma sprayed coating. Internal testing indicated that the parts may not have sufficient adhesion strength. The scope was identified to be all lots that were poro | 12 units | 2023-04-13 |
| Biomet, Inc. | UDI-DI | 2022-01-07 | Class II | Process control | The products in scope underwent an incorrect rework operation for the porous plasma sprayed coating. Internal testing indicated that the parts may not have sufficient adhesion strength. The scope was identified to be all lots that were poro | 12 units | 2023-04-13 |
| Biomet, Inc. | UDI-DI | 2022-01-07 | Class II | Process control | The products in scope underwent an incorrect rework operation for the porous plasma sprayed coating. Internal testing indicated that the parts may not have sufficient adhesion strength. The scope was identified to be all lots that were poro | 11 units | 2023-04-13 |
| Biomet, Inc. | 510(k) number | 2020-11-25 | Class II | Process control | Specific lots of multiple sterile medical devices may have a breach in the sterile seal. A breach in the packaging seal could lead to loss of sterility of the device. | 7428 | 2024-05-08 |
| Biomet, Inc. | 510(k) number | 2020-09-02 | Class II | Packaging process control | Product potentially being packaged without a taper adapter or baseplate. The package should contain one (1) baseplate and one (1) taper adapter, product may be packaged with two (2) baseplates and no (0) adapters or with no (0) baseplates a | 3 units | 2020-12-31 |
| Biomet, Inc. | 510(k) number | 2020-04-17 | Class II | Process control | Potential presence of elevated endotoxin levels that exceed the specification limit | 122 units | 2021-06-25 |
| Biomet, Inc. | 510(k) number | 2020-03-13 | Class II | Under Investigation by firm | There were unknown bioburden levels prior to sterilization, which may affect sterility of the product. | 125 | 2021-07-21 |
| Biomet, Inc. | 510(k) number | 2020-02-25 | Class II | Packaging process control | Package is intended to contain one (1) baseplate and one (1) taper adapter; however, devices may be packaged with two (2) baseplates and no (0) adapters. | 21 units | 2020-08-05 |
| Biomet, Inc. | 510(k) number | 2020-02-17 | Class II | Under Investigation by firm | A 15mm Shoulder Mini Humeral Stem was misidentified as a 9mm Shoulder Mini Humeral Stem. | 14 units | 2022-05-31 |
| Biomet, Inc. | 510(k) number | 2018-12-21 | Class II | Packaging process control | The product was potentially being packaged without a taper adapter. | 52 | 2020-05-06 |
| Biomet, Inc. | 510(k) number | 2018-10-10 | Class II | Under Investigation by firm | Zimmer Biomet is conducting a lot specific medical device recall for two lots of the Orthopedic Salvage System (OSS) and the Comprehensive Shoulder System. The investigation determined that the Mini Humeral Stem is potentially labeled as th | 3 total | 2020-04-28 |
| Biomet, Inc. | 510(k) number | 2017-12-08 | Class II | Under Investigation by firm | Zimmer Biomet is conducting a medical device recall for two lots of Comprehensive Humeral stems. The lots were commingled during the manufacturing process and were etched with incorrect lot numbers. The size difference between the two stem | 12 | 2018-09-04 |
| Biomet, Inc. | 510(k) number | 2017-12-08 | Class II | Under Investigation by firm | Zimmer Biomet is conducting a medical device recall for two lots of Comprehensive Humeral stems. The lots were commingled during the manufacturing process and were etched with incorrect lot numbers. The size difference between the two stem | 12 | 2018-09-04 |
| 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 | 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 | 2017-04-26 | Class II | Under Investigation by firm | Zimmer Biomet is conducting a voluntary recall for a single lot of the Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System after it was determined that two pieces from the lot were moved to finished goods and shipped des | 16 | 2018-03-30 |
| Biomet, Inc. | 510(k) number | 2017-02-17 | Class II | Process design | Endotoxin levels higher than process maximum limits were discovered in the identified polyethylene components. | 28,253 in total | 2018-01-29 |
| Biomet, Inc. | 510(k) number | 2016-12-20 | Class I | Device Design | Higher than anticipated rate of fracturing due to design. Risk of revision surgery due to fracturing. | 4388 | 2017-08-29 |
| Biomet, Inc. | 510(k) number | 2015-04-16 | Class III | Labeling mix-ups | Biomet hip joint, knee joint and shoulder joint replacement components device labeling contains incorrect GTIN (Global Trade Identification Number) codes. | 2 | 2016-05-16 |
| Biomet, Inc. | 510(k) number | 2015-01-07 | Class II | Process control | The taper adaptor is missing from the packaging, which may result in a delay in surgery greater than 30 minutes. | 11- 6 consumed, 5 with distributors | 2015-10-22 |
| Biomet, Inc. | 510(k) number | 2013-05-15 | Class II | Device Design | Biomet has initiated this action following an investigation which identified that the slot on the resection guide is offset in the wrong direction. When the slot on the resection guide is offset in the wrong direction, the Steinman pin that | 17 | 2014-06-09 |
| Biomet, Inc. | 510(k) number | 2011-04-22 | Not classified | Employee error | The firm is initiating this recall following an investigation which identified the rare possibility that certain units of Comprehensive Reverse Shoulder Humeral Trays may contain a locking ring that is incorrectly assembled. | 1,575 units all products | 2013-02-21 |
| Biomet, Inc. | 510(k) number | 2011-04-22 | Not classified | Employee error | The firm is initiating this recall following an investigation which identified the rare possibility that certain units of Comprehensive Reverse Shoulder Humeral Trays may contain a locking ring that is incorrectly assembled. | 1,575 units all products | 2013-02-21 |
| Biomet, Inc. | 510(k) number | 2011-04-22 | Not classified | Employee error | The firm is initiating this recall following an investigation which identified the rare possibility that certain units of Comprehensive Reverse Shoulder Humeral Trays may contain a locking ring that is incorrectly assembled. | 1575 all products | 2013-02-21 |
| Biomet, Inc. | 510(k) number | 2011-04-22 | Not classified | Employee error | The firm is initiating this recall following an investigation which identified the rare possibility that certain units of Comprehensive Reverse Shoulder Humeral Trays may contain a locking ring that is incorrectly assembled. | 1575 units all products | 2013-02-21 |
| Biomet, Inc. | 510(k) number | 2011-04-22 | Not classified | Employee error | The firm is initiating this recall following an investigation which identified the rare possibility that certain units of Comprehensive Reverse Shoulder Humeral Trays may contain a locking ring that is incorrectly assembled. | 1575 all products | 2013-02-21 |
| Biomet, Inc. | 510(k) number | 2011-04-22 | Not classified | Employee error | The firm is initiating this recall following an investigation which identified the rare possibility that certain units of Comprehensive Reverse Shoulder Humeral Trays may contain a locking ring that is incorrectly assembled. | 1575 all products | 2013-02-21 |
| Biomet, Inc. | 510(k) number | 2011-04-22 | Not classified | Employee error | The firm is initiating this recall following an investigation which identified the rare possibility that certain units of Comprehensive Reverse Shoulder Humeral Trays may contain a locking ring that is incorrectly assembled. | 1575 all products | 2013-02-21 |
| Biomet, Inc. | 510(k) number | 2011-04-22 | Not classified | Employee error | The firm is initiating this recall following an investigation which identified the rare possibility that certain units of Comprehensive Reverse Shoulder Humeral Trays may contain a locking ring that is incorrectly assembled. | 1575 all products. | 2013-02-21 |
| Biomet, Inc. | 510(k) number | 2011-04-22 | Not classified | Employee error | The firm is initiating this recall following an investigation which identified the rare possibility that certain units of Comprehensive Reverse Shoulder Humeral Trays may contain a locking ring that is incorrectly assembled. | 1,575 all products | 2013-02-21 |
| Biomet, Inc. | 510(k) number | 2011-04-22 | Not classified | Employee error | The firm is initiating this recall following an investigation which identified the rare possibility that certain units of Comprehensive Reverse Shoulder Humeral Trays may contain a locking ring that is incorrectly assembled. | 1575 all products | 2013-02-21 |
| Biomet, Inc. | 510(k) number | 2010-09-13 | Not classified | Pending | The firm received complaints regarding fracturing of the device. | 45 both products | 2011-07-27 |
| Biomet, Inc. | 510(k) number | 2010-09-13 | Not classified | Pending | The firm received complaints regarding fracturing of the device. | 45 both products | 2011-07-27 |
| Biomet, Inc. | 510(k) number | 2008-03-13 | Not classified | Device Design | The glenoid implant may not seat fully on the face of the natural glenoid due to inadequate measurement tolerances (tolerance stack-up) in the design of the cutter. Use of the instrument may lead to incomplete seating of the glenoid implan | 189 | 2008-10-15 |
| Biomet, Inc. | 510(k) number | 0012-12-06 | Class II | Nonconforming Material/Component | Biomet is recalling Part Number PT-113950 PT Hybrid Glenoid Post, following an investigation which identified that the male thread of the post may be oversized. This oversized condition can vary in degree and may lead to the following thre | 1050 | 2013-11-08 |
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.