Plate, Fixation, Bone

106 catalogue numbers from SP-2862, listed by Biomet Microfixation, United States, under Plate, Fixation, Bone. 22 manufacturers in China are registered for this product code.

Registry build 21.09.26
22manufacturers in China registered for this device type
106catalogue numbers in this listing
15510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (4), Zhejiang (3). 12 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HRS
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Kingj Medical Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Hangzhou Sino-MIM Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5
Beijing AK Medical Co., Ltd. Changping District Beijing Contract manufacturer 3

Showing 12 of 22. All 22 manufacturers in China registered for Plate, Fixation, Bone

Record

Regulatory record for Plate, Fixation, Bone
Listed by Biomet Microfixation, United States
FDA product code HRS
Device type Plate, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K091058
Record published 2015-10-11
Record revised 2025-05-30 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, serial number
Distribution end date 2020-07-27

Catalogue Numbers

Catalogue numbers for Plate, Fixation, Bone
Catalogue number Size Status
SP-2862 In distribution
69-6114 In distribution
69-6118 In distribution
69-6116 In distribution
69-6108 In distribution
69-6124 In distribution
SP-2860 In distribution
69-6110 In distribution
01-3900 In distribution
69-6128 In distribution
SP-2497 In distribution
01-3910 In distribution
323.0055 In distribution
SP-2499 In distribution
SP-2859 In distribution
69-6028 In distribution
01-3905 In distribution
323.1206 In distribution
SP-2503 In distribution
SP-1367 In distribution
SP-2861 In distribution
323.1006 In distribution
69-6008 In distribution
SP-2496 In distribution
69-6012 In distribution
01-3801 In distribution
69-6010 In distribution
69-6018 In distribution
323.0071 In distribution
69-6122 In distribution
73-1301-03 In distribution
69-6126 In distribution
SP-2864 In distribution
01-3906 In distribution
SP-2501 In distribution
69-6024 In distribution
SP-2865 In distribution
323.1031 In distribution
69-6022 In distribution
69-6014 In distribution
323.1004 In distribution
69-6120 In distribution
SP-2498 In distribution
323.1003 In distribution
69-6026 In distribution
SP-2863 In distribution
323.1203 In distribution
69-6020 In distribution
323.1032 In distribution
323.1001 In distribution
69-6016 In distribution
SP-2869 In distribution
323.1013 In distribution
323.1002 In distribution
323.1201 In distribution
SP-3139 In distribution
SP-2868 In distribution
69-6112 In distribution
SP-2505 In distribution
69-6010 Withdrawn
69-6108 Withdrawn
69-6008 Withdrawn
SP-2864 Withdrawn
SP-2497 Withdrawn
69-6012 Withdrawn
SP-2496 Withdrawn
SP-2505 Withdrawn
SP-2503 Withdrawn
69-6026 Withdrawn
69-6018 Withdrawn
SP-2500 Withdrawn
69-6126 Withdrawn
69-6110 Withdrawn
SP-2860 Withdrawn
SP-2501 Withdrawn
69-6024 Withdrawn
SP-2867 Withdrawn
69-6124 Withdrawn
69-6122 Withdrawn
69-6114 Withdrawn
SP-2868 Withdrawn
SP-2865 Withdrawn
SP-2869 Withdrawn
69-6028 Withdrawn
SP-2506 Withdrawn
69-6118 Withdrawn
SP-2498 Withdrawn
SP-2502 Withdrawn
01-3802 Withdrawn
SP-3139 Withdrawn
69-6116 Withdrawn
SP-2859 Withdrawn
69-6020 Withdrawn
69-6014 Withdrawn
SP-2504 Withdrawn
69-6022 Withdrawn
69-6112 Withdrawn
SP-2862 Withdrawn
73-1300-03 Withdrawn
69-6128 Withdrawn
SP-2499 Withdrawn
SP-2863 Withdrawn
SP-2866 Withdrawn
69-6120 Withdrawn
SP-2861 Withdrawn
69-6016 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pectus System Biomet Microfixation 4,662
Arthrex® Arthrex, Inc. 3,031
Evos Smith & Nephew, Inc. 2,235
Peri-Loc Smith & Nephew, Inc. 2,196
OsteoMed Osteomed 1,961
VariAx Stryker GmbH 1,934
Aptus Medartis Inc. 1,688
TC-100 Smith & Nephew, Inc. 1,639
Plate, Fixation, Bone Synthes Gmbh 1,613
Anthem Globus Medical, Inc. 1,551
Acumed Acumed LLC 1,360
Signex Osteonic Co., Ltd. 1,310

Showing 12 of 3,530. All products under Plate, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K261002 2026-06-02
K241709 2024-09-19
K212782 2022-05-17
K212608 2022-04-22
K213712 2022-03-11
K162974 2016-12-09
K163007 2016-11-23
K161896 2016-08-02
K152253 2016-03-24
K151019 2015-11-03
K142823 2015-02-25
K121302 2012-09-19
K110574 2011-05-18
K091058 2009-07-22
K071577 2007-09-06

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 Plate, Fixation, Bone
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet Microfixation 510(k) number 2011-11-23 Not classified Device Design Biomet Microfixation, Inc., Jacksonville, FL recalled their SternaLock Blu Implant Tray on 11/23/11, model numbers 73-1300 through 73-1302 due to the possibility of an inaccurate reading on the Screw Measuring Area. If used incorrectly, the 109 trays 2012-04-03

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
2009-03-20 Not classified Device Design This recall is based on the occurrence of known adverse effects identified in the device instructions for use. Bending, fracture, loosening, rubbing and migration of the devices can occur as a result of excessive activity, trauma or load b 2,117 2009-09-11

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