Plate, Bone

215 catalogue numbers from PM619196, 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
215catalogue 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 Plate, Bone
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) K113512
Record published 2017-03-15
Record revised 2025-06-09 (version 9)

Specifications

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
Distribution end date 2020-07-27

Catalogue Numbers

Catalogue numbers for Plate, Bone
Catalogue number Size Status
PM619196 In distribution
SP-2358 In distribution
PM619603 In distribution
PM619200 In distribution
SP-1947 In distribution
PM619568 In distribution
PM619334 In distribution
MP-0120 In distribution
SP-1487 In distribution
SP-2730 In distribution
SP-1818 In distribution
SP-1525 In distribution
MP-0111 In distribution
31-3100 In distribution
MP-0107 In distribution
SP-1488 In distribution
SP-2243 In distribution
SP-1397 In distribution
SP-1002 In distribution
SP-2258 In distribution
SP-2754 In distribution
PM619309-A In distribution
MP-0165 In distribution
MP-0155 In distribution
SP-1644 In distribution
PM619341-A In distribution
PM619321-A In distribution
SP-2726 In distribution
SP-1751 In distribution
PM619450 In distribution
SP-1640 In distribution
SP-1483 In distribution
SP-1396 In distribution
PM619148 In distribution
PM619212 In distribution
MP-0146 In distribution
SP-2878 In distribution
MP-0126 In distribution
46-2464 In distribution
SP-1546 In distribution
SP-2583 In distribution
SP-3335 In distribution
SP-1486 In distribution
SP-3029 In distribution
915-3110 In distribution
SP-1749 In distribution
SP-2729 In distribution
MP-0141-03 In distribution
SP-3067 In distribution
SP-1865 In distribution
SP-1482 In distribution
MP-0122 In distribution
SP-2750 In distribution
15-0281 In distribution
MP-0157 In distribution
SP-1847 In distribution
MP-0137 In distribution
PM619206 In distribution
SP-1485 In distribution
MP-0129 In distribution
MP-0141-01 In distribution
SP-1894 In distribution
PM619579-A In distribution
SP-1492 In distribution
MP-0105 In distribution
MP-0115 In distribution
SP-2748 In distribution
MP-0158 In distribution
SP-2243 In distribution
SP-1238 In distribution
SP-1639 In distribution
SP-3030 In distribution
SP-1654 In distribution
MP-0138 In distribution
MP-0161 In distribution
SP-2745 In distribution
PM619434 In distribution
PM619552 In distribution
SP-1545 In distribution
PM619521-A In distribution
PM619442 In distribution
SP-1491 In distribution
SP-1395 In distribution
SP-2747 In distribution
SP-3391 In distribution
MP-0416 In distribution
MP-0153 In distribution
PM619428 In distribution
SP-2738 In distribution
SP-1378 In distribution
SP-2582 In distribution
MP-0135 In distribution
SP-1423 In distribution
MP-0101 In distribution
SP-1980 In distribution
SP-2740 In distribution
SP-1895 In distribution
PM619581 In distribution
SP-2574 In distribution
SP-1837 In distribution
SP-1548 In distribution
SP-1237 In distribution
SP-1150 In distribution
SP-1489 In distribution
PM619326 In distribution
SP-2193-T In distribution
SP-1843 In distribution
PP-0299 In distribution
24-1189 In distribution
SP-1920 In distribution
SP-2739 In distribution
MP-0144 In distribution
MP-0163 In distribution
15-0280 In distribution
SP-1896 In distribution
SP-2751 In distribution
SP-1666 In distribution
SP-3146 In distribution
SP-1897 In distribution
SP-1762 In distribution
SP-1213 In distribution
SP-1645 In distribution
PP-0301 In distribution
01-2556 In distribution
SP-1490 In distribution
SP-1524 In distribution
SP-2728 In distribution
01-9011 In distribution
SP-2746 In distribution
SP-1398 In distribution
SP-2357 In distribution
SP-2468 In distribution
SP-2732 In distribution
PP-0360 In distribution
PM619587 In distribution
MP-0117 In distribution
MP-0124 In distribution
SP-2356 In distribution
PM619599 In distribution
SP-1547 In distribution
MP-0113 In distribution
SP-2741 In distribution
PM619419 In distribution
SP-1526 In distribution
SP-2584 In distribution
SP-1481 In distribution
SP-2731 In distribution
SP-1343 In distribution
PM619577 In distribution
SP-1523 In distribution
PP-0296 In distribution
MP-0149 In distribution
SP-1484 In distribution
PM619430 In distribution
SP-2755 In distribution
SP-2749 In distribution
MP-0414 In distribution
SP-2752 In distribution
SP-3388 In distribution
MP-0098 In distribution
PP-0319 In distribution
SP-3334 In distribution
SP-2355 In distribution
SP-2422 In distribution
SP-3193 In distribution
SP-2753 In distribution
PM619597 In distribution
MP-0109 In distribution
SP-1895 Withdrawn
SP-3146 Withdrawn
SP-2747 Withdrawn
SP-2746 Withdrawn
01-7106-MP-R Withdrawn
SP-3030 Withdrawn
SP-1998 Withdrawn
SP-1865 Withdrawn
46-2464 Withdrawn
01-9011 Withdrawn
SP-2749 Withdrawn
SP-2754 Withdrawn
SP-2827 Withdrawn
SP-2467 Withdrawn
01-7106-MP-L Withdrawn
SP-1747 Withdrawn
SP-1837 Withdrawn
SP-1896 Withdrawn
SP-2750 Withdrawn
24-1189 Withdrawn
SP-3067 Withdrawn
SP-2422 Withdrawn
SP-2878 Withdrawn
SP-2755 Withdrawn
SP-3029 Withdrawn
SP-2845 Withdrawn
SP-2752 Withdrawn
SP-2000 Withdrawn
SP-2745 Withdrawn
SP-1836 Withdrawn
01-7108-MP-R Withdrawn
SP-2748 Withdrawn
SP-1914 Withdrawn
SP-1920 Withdrawn
SP-2751 Withdrawn
SP-2846 Withdrawn
SP-1848 Withdrawn
SP-1654 Withdrawn
SP-1915 Withdrawn
SP-1894 Withdrawn
SP-2258 Withdrawn
SP-1897 Withdrawn
SP-1863 Withdrawn
SP-2469 Withdrawn
SP-2726 Withdrawn
SP-2753 Withdrawn
01-7108-MP-L 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

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

Recalls naming the identifiers of Plate, Bone
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet, Inc. 510(k) number 2017-01-10 Class II Under Investigation by firm The identification of the devices was non-conforming with off-centered slots and the no-go gage starting in the pilot hole. 11 2018-03-26
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 2009-11-06 Not classified Process change control The Twist Drill 1.1x50mm, 3.5mm stop, with J notch Lots #’s 537407, 536306, and 535933 which were packaged and shipped without the instructions for use (IFU). 283 pieces 2010-03-02
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