Comprehensive® SRS Instrument

36 catalogue numbers from 405143, listed by Biomet Orthopedics, United States, under Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
36catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Shanghai (3), Zhejiang (1), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code MBF
Manufacturer City Province Registered as Device types
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
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

Record

Regulatory record for Comprehensive® SRS Instrument
Listed by Biomet Orthopedics, United States
FDA product code MBF
Device type Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented
Device class Class 2
Regulation 21 CFR 888.3670
510(k) K111746
Record published 2021-11-05
Record revised 2025-05-30 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Comprehensive® SRS Instrument
Catalogue number Size Status
405143 In distribution
405101 SMALL 48MM In distribution
405205 15MM X 100MM In distribution
405201 19 mm X 75 mm In distribution
405171 9 mm X 150 mm In distribution
405198 16 mm X 75 mm In distribution
405174 11MM X 100MM In distribution
405196 13 mm X 75 mm In distribution
405128 8MM X 150MM In distribution
405206 16 mm X 100 mm In distribution
405169 9 mm X 75 mm In distribution
405140 RIGHT 60MM In distribution
405106 62 mm Large In distribution
405130 12MM X 150MM In distribution
405134 10MM X 200MM In distribution
405202 20MM X 75MM In distribution
405128 8 mm X 150 mm In distribution
405169 9MM X 75MM In distribution
405174 11 mm X 100 mm In distribution
405107 TUMOR 51MM In distribution
405215 5MM X 200MM In distribution
405207 17 mm X 100 mm In distribution
405143 In distribution
405136 LEFT 50MM In distribution
405203 7 mm X 100 mm In distribution
405108 61 mm In distribution
405127 6 mm X 150 mm In distribution
405181 LARGE In distribution
405117 8MM X 75MM In distribution
405173 11MM X 75MM In distribution
405122 8MM X 100MM In distribution
405206 16MM X 100MM In distribution
405176 11MM X 200MM In distribution
405217 13MM X 200MM In distribution
405218 14 mm X 200 mm In distribution
405126 4MM X 150MM In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Shoulder Innovations Inset Reverse Total Shoulder Shoulder Innovations, Inc 181
Shoulder Innovations Humeral Short Stem System Shoulder Innovations, Inc 87
Comprehensive® Shoulder System Biomet Orthopedics 70
BIO-Modular Shoulder System Biomet Orthopedics 41
Shoulder Innovations InSet 95 Humeral Stem Shoulder Innovations, Inc 40
Identity™ Zimmer, Inc. 29
Comprehensive® SRS Biomet Orthopedics 25
Inhance Depuy (Ireland) 25
SMR Shoulder Limacorporate 20
Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented Synthes (U.S.A.) LP 19
BI-Angular System Biomet Orthopedics 16
Global Unite Depuy (Ireland) 16

Showing 12 of 71. All products under Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K112905 2012-05-24

Recalls Naming This Product

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

Recalls naming the identifiers of Comprehensive® SRS Instrument
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet, Inc. 510(k) number 2018-02-28 Class II Under Investigation by firm During assembly, an SRS Humeral Distal Body implant failed to engage correctly at the point of reduction with a Discovery Elbow System Humeral Condyle. A mismatch between the screw holes in the Humeral Body & Elbow Condyle affects assembly 634 2020-08-11
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 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

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