TraumaOne System

357 catalogue numbers from 41-2312, listed by Biomet Microfixation, United States, under Plate, Bone. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
357catalogue numbers in this listing
8510(k) clearances naming this product code
10recalls on this code

Who Else Makes It

Concentrated in Jiangsu (1), Shanghai (1), Shaanxi (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 JEY
Manufacturer City Province Registered as Device types
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Kontour (Xi’an) Medical Technology Co., Ltd. Xi’An Shaanxi Contract manufacturer 4

Record

Regulatory record for TraumaOne System
Listed by Biomet Microfixation, United States
FDA product code JEY
Device type Plate, Bone
Device class Class 2
Regulation 21 CFR 872.4760
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K081067
Record published 2020-06-17
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
Distribution end date 2020-07-30

Catalogue Numbers

Catalogue numbers for TraumaOne System
Catalogue number Size Status
41-2312 In distribution
SP-2998-PBL In distribution
SP-3211-L In distribution
SP-3009 In distribution
46-2462 In distribution
41-2410 In distribution
SP-3200 In distribution
45-2110 In distribution
SP-2292 In distribution
41-2710 In distribution
41-2207 In distribution
45-2406 In distribution
41-2118 In distribution
SP-3294 In distribution
41-2018 In distribution
SP-3210-L In distribution
41-2708 In distribution
SP-3248 In distribution
SP-2284 In distribution
42-1003 In distribution
45-2312 In distribution
SP-3059 In distribution
SP-2619 In distribution
45-2410 In distribution
SP-3207 In distribution
SP-2838 In distribution
45-2108 In distribution
SP-3201 In distribution
SP-3386 In distribution
SP-2566 In distribution
SP-2714 In distribution
45-2012 In distribution
SP-2588T In distribution
SP-3209-R In distribution
45-2118 In distribution
SP-3032 In distribution
45-2006 In distribution
SP-3204 In distribution
SP-3056 In distribution
43-1001 In distribution
41-2314 In distribution
SP-2291 In distribution
SP-3053 In distribution
SP-2916T In distribution
91-5711 In distribution
45-2412 In distribution
SP-2908 In distribution
44-1002 In distribution
SP-2705 In distribution
41-2712 In distribution
41-2205 In distribution
SP-2981 In distribution
01-0292 In distribution
SP-3210-R In distribution
SP-2978 In distribution
SP-3205 In distribution
SP-3036 In distribution
SP-3000-PBR In distribution
44-1024 In distribution
SP-2276 In distribution
41-2306 In distribution
41-2305 In distribution
43-1008 In distribution
41-2318 In distribution
SP-2851 In distribution
01-7039 In distribution
01-7038 In distribution
45-2414 In distribution
SP-2667 In distribution
SP-3058 In distribution
45-2018 In distribution
SP-3000-PBL In distribution
SP-3202 In distribution
41-2116 In distribution
41-2408 In distribution
44-1001 In distribution
SP-3054 In distribution
SP-2979 In distribution
SP-3301 In distribution
41-2108 In distribution
SP-2375 In distribution
SP-3209-L In distribution
44-1012 In distribution
41-2014 In distribution
44-1023 In distribution
01-7121 In distribution
43-1007 In distribution
SP-2704 In distribution
SP-3196 In distribution
SP-2703 In distribution
41-2716 In distribution
SP-3031 In distribution
SP-3070 In distribution
45-2114 In distribution
45-2106 In distribution
41-2416 In distribution
SP-3208-R In distribution
SP-2618 In distribution
41-2412 In distribution
41-2016 In distribution
41-2114 In distribution
SP-2376 In distribution
SP-2575 In distribution
SP-3206 In distribution
41-2006 In distribution
SP-2630 In distribution
SP-2465 In distribution
SP-2608 In distribution
41-2714 In distribution
45-2416 In distribution
SP-2528 In distribution
41-2316 In distribution
45-2112 In distribution
SP-2999-PBR In distribution
41-2406 In distribution
SP-2604 In distribution
44-1018 In distribution
SP-2609 In distribution
SP-2256 In distribution
45-2010 In distribution
SP-2194 In distribution
45-2008 In distribution
44-1021 In distribution
41-2012 In distribution
42-1016 In distribution
SP-2697 In distribution
SP-3034 In distribution
41-2005 In distribution
45-2305 In distribution
SP-3247 In distribution
SP-2605 In distribution
43-1004 In distribution
45-2316 In distribution
45-2314 In distribution
41-2310 In distribution
41-2112 In distribution
41-2414 In distribution
45-2306 In distribution
42-1002 In distribution
SP-2631 In distribution
SP-3221 In distribution
SP-3211-R In distribution
SP-3203 In distribution
42-1006 In distribution
45-2116 In distribution
SP-2893 In distribution
SP-3295 In distribution
SP-2839 In distribution
SP-2585 In distribution
45-2418 In distribution
01-7123 In distribution
SP-3208-L In distribution
43-1005 In distribution
42-1007 In distribution
SP-2999-PBL In distribution
SP-2527 In distribution
45-2310 In distribution
41-2308 In distribution
SP-2623 In distribution
01-8681 In distribution
SP-2402 In distribution
SP-2526 In distribution
45-2016 In distribution
45-2014 In distribution
43-1021 In distribution
44-1022 In distribution
SP-2665 In distribution
41-2110 In distribution
41-2008 In distribution
43-1016 In distribution
42-1004 In distribution
SP-2397 In distribution
41-2418 In distribution
SP-2724 In distribution
41-2010 In distribution
42-1005 In distribution
44-1005 In distribution
45-2308 In distribution
SP-2587 In distribution
SP-2586 In distribution
SP-3057 In distribution
SP-2610 In distribution
01-7122 In distribution
91-5707 In distribution
41-2718 In distribution
45-2318 In distribution
45-2408 In distribution
45-2005 In distribution
41-2106 In distribution
SP-2528 Withdrawn
45-2108 Withdrawn
45-2114 Withdrawn
SP-3201 Withdrawn
41-2116 Withdrawn
SP-3210-L Withdrawn
SP-2292 Withdrawn
SP-3211-R Withdrawn
43-1007 Withdrawn
41-2014 Withdrawn
SP-2402 Withdrawn
45-2118 Withdrawn
41-2008 Withdrawn
SP-2838 Withdrawn
45-2008 Withdrawn
01-7122 Withdrawn
SP-3053 Withdrawn
SP-3248 Withdrawn
SP-2979 Withdrawn
41-2110 Withdrawn
42-1007 Withdrawn
45-2016 Withdrawn
SP-2665 Withdrawn
SP-3206 Withdrawn
SP-2609 Withdrawn
41-2106 Withdrawn
45-2306 Withdrawn
45-2416 Withdrawn
SP-3205 Withdrawn
45-2418 Withdrawn
45-2005 Withdrawn
43-1001 Withdrawn
SP-3222 Withdrawn
44-1023 Withdrawn
SP-3009 Withdrawn
SP-2893 Withdrawn
41-2406 Withdrawn
41-2306 Withdrawn
41-2410 Withdrawn
SP-3208-R Withdrawn
41-2712 Withdrawn
41-2710 Withdrawn
41-2207 Withdrawn
45-2414 Withdrawn
SP-3059 Withdrawn
41-2018 Withdrawn
91-5707 Withdrawn
45-2110 Withdrawn
44-1022 Withdrawn
SP-3031 Withdrawn
45-2006 Withdrawn
45-2318 Withdrawn
41-2010 Withdrawn
41-2112 Withdrawn
45-2312 Withdrawn
45-2310 Withdrawn
SP-2631 Withdrawn
44-1002-PB1 Withdrawn
41-2012 Withdrawn
41-2714 Withdrawn
SP-3209-R Withdrawn

Showing 250 of 300 catalogue numbers.

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Plate, Bone Stryker Leibinger Gmbh & Co. KG 1,338
Level ONE CMF KLS-Martin L.P. 1,160
Medicon Medicon eG. Chirurgiemechaniker-Genossenschaft 843
OsteoMed Osteomed 675
Bioplate® Bioplate, Inc. 669
Plate, Bone Synthes Gmbh 568
Leforte System Bone Plate Jeil Medical Corporation 466
CMF Visionare Visionare LLC 421
Level ONE CMF, Sterile KLS-Martin L.P. 416
Faico CMF System Faico Medical, LLC 361
MatrixMANDIBLE Synthes Gmbh 277
Level ONE Neuro KLS-Martin L.P. 253

Showing 12 of 152. All products under Plate, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K202969 2021-08-05
K152326 2015-12-10
K143336 2015-04-01
K132600 2013-10-02
K131674 2013-08-08
K121589 2012-09-21
K113512 2012-06-29
K081067 2008-05-09

Recalls Naming This Product

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

Recalls naming the identifiers of TraumaOne System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet Microfixation 510(k) number 2015-08-06 Class II Component change control The lids on implant caddies within P/N 17-5000 and 19-5000 could not be opened by the user without application of undesirable/unexpected excessive force. 37 cases 2017-10-13
Biomet Microfixation 510(k) number 2015-08-06 Class II Component change control The lids on implant caddies within P/N 17-5000 and 19-5000 could not be opened by the user without application of undesirable/unexpected excessive force. 5 units 2017-10-13
Biomet Microfixation 510(k) number 2010-08-31 Not classified Other Mislabeled size: The 2.0/1.0 4 hole long plate, Lot 120150 is labeled as 01-9205 (2.0/1.0 4 Hole Long Plate), however, the package contains a 01-9204 (2.0/1.0 4 Hole Regular Plate). 56 2010-11-19
Biomet Microfixation 510(k) number 2010-07-28 Not classified Labeling mix-ups Biomet Microfixation, Jacksonville, FL is recalling their 1.5 6 Hole Reg Double Y, Lots 785710, 753120, 693500 and 733600. This product is labeled as 01-7110-K (1.5 6 Hole Reg Double Y), however the package contains a 01-7112-K (1.5.6 Hold 180 2011-06-24
Biomet Microfixation 510(k) number 2010-04-26 Not classified Error in labeling On 4/26/10 Biomet Microfixation, Jacksonville, FL initiated a recall of their 1.5 3/3 hole 100 degree left X-long L plate, Model #01-7036, Lot #193690. Product is labeled incorrectly. 23 2012-04-18
Biomet Microfixation 510(k) number 2009-10-06 Not classified Process control Biomet Microfixation is recalling Model 01-7293 an Model 99-7293-01, 1.5X3.5mm Self Drilling, Low Profile, Cross Drive screw, 5/PK was found to contain a 91-6104 (1.5X4mm High Torque, Self Drilling, Cross Drive screw. 831 screws 2010-04-07
Biomet Microfixation 510(k) number 2009-10-05 Not classified Process design Biomet Microfixation is recalling 91-6103 1.5×3.5mm HT SD X-drive screw Lot Number 829760. This package may contain 91-6704 1.5x4mm ThinFlap SD X-drive screw. 91 units 2010-12-15

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
2008-07-11 Not classified Labeling mix-ups The packaging for the 91-2416, 2.4X16MM HT X-DRIVE SCREW, Lot 493200 actually contained the 99-6577, 2.0X7MM FOSSA X-DRIVE SCREW. 10 2009-09-11
2008-03-19 Not classified Packaging process control The outer foil pouch on the Lactosorb Plate system was not properly sealed. The product is labeled as sterile, but the lot was not sterilized. These devices are intended to be implanted into bone and are required to be sterile. A heavy b 117 2009-09-11
2006-02-17 Not classified Device Design Lorenz Engineer discovered flex tube could break if bent too much. 34 pieces 2011-12-12
2006-02-17 Not classified Device Design Lorenz Engineer discovered flex tube could break if bent too much. 41 pieces and 31 pieces respectively 2011-12-12
2006-02-17 Not classified Device Design Lorenz Engineer discovered flex tube could break if bent too much. 76 pieces 2011-12-12

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