2.0 System

173 catalogue numbers from SP-2205, 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
173catalogue 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 2.0 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) K121589
Record published 2020-03-27
Record revised 2025-06-09 (version 8)

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
Distribution end date 2020-07-27

Catalogue Numbers

Catalogue numbers for 2.0 System
Catalogue number Size Status
SP-2205 In distribution
SP-3158 In distribution
95-2315 In distribution
SP-3276 In distribution
SP-3347 In distribution
SP-3155 In distribution
SP-3284 In distribution
SP-1735 In distribution
95-2311 In distribution
SP-3348 In distribution
SP-3266 In distribution
SP-3265 In distribution
SP-2204 In distribution
SP-1703 In distribution
91-2021 In distribution
SP-3173 In distribution
SP-3289 In distribution
95-2011 In distribution
01-9086 In distribution
91-2311 In distribution
SP-3172 In distribution
95-2019 In distribution
SP-3154 In distribution
95-2017 In distribution
SP-3271 In distribution
SP-2217 In distribution
SP-3153 In distribution
SP-3181 In distribution
SP-2208 In distribution
SP-3178 In distribution
SP-3270 In distribution
SP-1704 In distribution
SP-3159 In distribution
SP-3174 In distribution
SP-3180 In distribution
SP-2203 In distribution
SP-3263 In distribution
91-2317 In distribution
91-2017 In distribution
95-2019T In distribution
01-9285 In distribution
95-2313 In distribution
91-2309 In distribution
SP-3282 In distribution
SP-3287 In distribution
SP-2209L In distribution
SP-2213 In distribution
SP-3152 In distribution
SP-3291 In distribution
SP-3157 In distribution
SP-1702 In distribution
SP-3156 In distribution
SP-3280 In distribution
SP-3345 In distribution
SP-3175 In distribution
SP-3281 In distribution
SP-3346 In distribution
95-2009 In distribution
95-2015 In distribution
SP-3171 In distribution
SP-3286 In distribution
91-2015 In distribution
SP-2219R In distribution
SP-3273 In distribution
SP-3262 In distribution
SP-3166 In distribution
SP-3275 In distribution
91-2019 In distribution
SP-3279 In distribution
SP-3170 In distribution
SP-3161 In distribution
95-2309 In distribution
SP-3179 In distribution
SP-2207 In distribution
SP-3278 In distribution
SP-2202 In distribution
SP-2216 In distribution
SP-3283 In distribution
95-2317 In distribution
91-2013 In distribution
SP-3267 In distribution
SP-3264 In distribution
91-2029 In distribution
91-2019T In distribution
SP-3272 In distribution
SP-3285 In distribution
SP-2206 In distribution
SP-3277 In distribution
SP-3162 In distribution
SP-2212 In distribution
SP-3167 In distribution
SP-3290 In distribution
SP-1738 In distribution
SP-3160 In distribution
SP-3165 In distribution
SP-2215 In distribution
91-2011 In distribution
SP-3163 In distribution
SP-3176 In distribution
SP-3168 In distribution
SP-2200 In distribution
SP-3274 In distribution
SP-3268 In distribution
SP-3177 In distribution
91-2315 In distribution
SP-3169 In distribution
01-9278 In distribution
SP-1736 In distribution
95-2013 In distribution
SP-2214 In distribution
SP-2210 In distribution
91-2009 In distribution
SP-3288 In distribution
SP-2218 In distribution
SP-3269 In distribution
SP-1737 In distribution
SP-3164 In distribution
91-2313 In distribution
SP-1737 Withdrawn
SP-2212 Withdrawn
SP-3153 Withdrawn
SP-3164 Withdrawn
SP-1702 Withdrawn
SP-2215 Withdrawn
SP-3152 Withdrawn
SP-3165 Withdrawn
SP-3155 Withdrawn
SP-3172 Withdrawn
SP-3177 Withdrawn
SP-2213 Withdrawn
SP-3176 Withdrawn
SP-2209L Withdrawn
SP-2205 Withdrawn
SP-2207 Withdrawn
SP-2204 Withdrawn
SP-2203 Withdrawn
SP-3170 Withdrawn
SP-3169 Withdrawn
SP-2214 Withdrawn
SP-2206 Withdrawn
SP-3168 Withdrawn
SP-1704 Withdrawn
SP-2217 Withdrawn
SP-2208 Withdrawn
SP-3158 Withdrawn
SP-1736 Withdrawn
SP-3161 Withdrawn
SP-3154 Withdrawn
SP-3174 Withdrawn
SP-3159 Withdrawn
SP-1738 Withdrawn
SP-2202 Withdrawn
SP-2210 Withdrawn
SP-3171 Withdrawn
SP-3157 Withdrawn
SP-3181 Withdrawn
SP-1703 Withdrawn
SP-3166 Withdrawn
SP-3180 Withdrawn
SP-2216 Withdrawn
SP-2218 Withdrawn
SP-3178 Withdrawn
SP-3167 Withdrawn
SP-2219R Withdrawn
SP-2200 Withdrawn
SP-3175 Withdrawn
SP-3160 Withdrawn
SP-3173 Withdrawn
SP-3179 Withdrawn
SP-1735 Withdrawn
SP-3156 Withdrawn
SP-3162 Withdrawn
SP-3163 Withdrawn

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
TraumaOne System Biomet Microfixation 357
MatrixMANDIBLE Synthes Gmbh 277

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

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

Recalls naming the identifiers of 2.0 System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
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