Phoenix Retrograde Nail System

73 catalogue numbers from 14-444146, listed by Biomet Orthopedics, United States, under Rod, Fixation, Intramedullary And Accessories. 17 manufacturers in China are registered for this product code.

Registry build 21.09.26
17manufacturers in China registered for this device type
73catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (3), Zhejiang (3). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HSB
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
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
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

Showing 12 of 17. All 17 manufacturers in China registered for Rod, Fixation, Intramedullary And Accessories

Record

Regulatory record for Phoenix Retrograde Nail System
Listed by Biomet Orthopedics, United States
FDA product code HSB
Device type Rod, Fixation, Intramedullary And Accessories
Device class Class 2
Regulation 21 CFR 888.3020
510(k) K072161
Record published 2015-10-24
Record revised 2025-05-30 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Phoenix Retrograde Nail System
Catalogue number Size Status
14-444146 9 MM 460 MM In distribution
14-444334 12 MM 340 MM In distribution
14-444539 15 MM 390 MM In distribution
14-444138 9 MM 380 MM In distribution
14-444142 9 MM 420 MM In distribution
14-444442 13.5 MM 420 MM In distribution
14-444525 15 MM 250 MM In distribution
14-444234 10.5 MM 340 MM In distribution
14-444132 9 MM 320 MM In distribution
14-444545 15 MM 450 MM In distribution
14-444428 13.5 MM 280 MM In distribution
14-444446 13.5 MM 460 MM In distribution
14-444332 12 MM 320 MM In distribution
14-444444 13.5 MM 440 MM In distribution
14-444534 15 MM 340 MM In distribution
14-444144 9 MM 440 MM In distribution
14-444230 10.5 MM 300 MM In distribution
14-444246 10.5 MM 460 MM In distribution
14-444224 10.5 MM 240 MM In distribution
14-444432 13.5 MM 320 MM In distribution
14-444536 15 MM 360 MM In distribution
14-444344 12 MM 440 MM In distribution
14-444540 15 MM 400 MM In distribution
14-444529 15 MM 290 MM In distribution
14-444346 12 MM 460 MM In distribution
14-444541 15 MM 410 MM In distribution
14-444326 12 MM 260 MM In distribution
14-444548 15 MM 480 MM In distribution
14-444242 10.5 MM 420 MM In distribution
14-444324 12 MM 240 MM In distribution
14-444524 15 MM 240 MM In distribution
14-444537 15 MM 370 MM In distribution
14-444130 9 MM 300 MM In distribution
14-444532 15 MM 320 MM In distribution
14-444546 15 MM 460 MM In distribution
14-444430 13.5 MM 300 MM In distribution
14-444342 12 MM 420 MM In distribution
14-444136 9 MM 360 MM In distribution
14-444526 15 MM 260 MM In distribution
14-444531 15 MM 310 MM In distribution
14-444535 15 MM 350 MM In distribution
14-444140 9 MM 400 MM In distribution
14-444543 15 MM 430 MM In distribution
14-444124 9 MM 240 MM In distribution
14-444226 10.5 MM 260 MM In distribution
14-444134 9 MM 340 MM In distribution
14-444436 13.5 MM 360 MM In distribution
14-444538 15 MM 380 MM In distribution
14-444240 10.5 MM 400 MM In distribution
14-444424 13.5 MM 240 MM In distribution
14-444547 15 MM 470 MM In distribution
14-444434 13.5 MM 340 MM In distribution
14-444328 12 MM 280 MM In distribution
14-444533 15 MM 330 MM In distribution
14-444426 13.5 MM 260 MM In distribution
14-444236 10.5 MM 360 MM In distribution
14-444228 10.5 MM 280 MM In distribution
14-444527 15 MM 270 MM In distribution
14-444340 12 MM 400 MM In distribution
14-444440 13.5 MM 400 MM In distribution
14-444542 15 MM 420 MM In distribution
14-444244 10.5 MM 440 MM In distribution
14-444238 10.5 MM 380 MM In distribution
14-444338 12 MM 380 MM In distribution
14-444528 15 MM 280 MM In distribution
14-444330 12 MM 300 MM In distribution
14-444128 9 MM 280 MM In distribution
14-444336 12 MM 360 MM In distribution
14-444530 15 MM 300 MM In distribution
14-444232 10.5 MM 320 MM In distribution
14-444544 15 MM 440 MM In distribution
14-444438 13.5 MM 380 MM In distribution
14-444126 9 MM 260 MM In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
T2 Stryker GmbH 1,373
Autobahn Globus Medical, Inc. 1,258
Gamma Stryker GmbH 1,120
Summa Orthopaedics Femur Nail System Jeil Medical Corporation 742
Arix Femur Nail System Jeil Medical Corporation 742
Orthofix Orthofix SRL 721
Rod, Fixation, Intramedullary And Accessories Synthes Gmbh 715
Trigen Smith & Nephew, Inc. 681
Arthrex® Arthrex, Inc. 665
Precice® Intramedullary Limb Lengthening System NuVasive Specialized Orthopedics, Inc. 596
Apex Orthoxel Designated Activity Company 569
Natural Nail® Zimmer, Inc. 552

Showing 12 of 2,207. All products under Rod, Fixation, Intramedullary And Accessories

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K070955 2007-10-12
K013923 2002-02-25
K002278 2000-10-23
K002057 2000-10-04

Recalls Naming This Product

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

Recalls naming the identifiers of Phoenix Retrograde Nail System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
EBI, LLC 510(k) number 2009-04-02 Not classified Nonconforming Material/Component Some devices could have been made with raw material lots that may have inclusions, and could result in decreased strength of the device. 16 2009-09-23
EBI, LLC 510(k) number 2009-04-02 Not classified Nonconforming Material/Component Some devices could have been made with raw material lots that may have inclusions, and could result in decreased strength of the device. 27 2009-09-23
EBI, LLC 510(k) number 2009-04-02 Not classified Nonconforming Material/Component Some devices could have been made with raw material lots that may have inclusions, and could result in decreased strength of the device. 25 2009-09-23
EBI, LLC 510(k) number 2009-04-02 Not classified Nonconforming Material/Component Some devices could have been made with raw material lots that may have inclusions, and could result in decreased strength of the device. 32 2009-09-23
EBI, LLC 510(k) number 2009-04-02 Not classified Nonconforming Material/Component Some devices could have been made with raw material lots that may have inclusions, and could result in decreased strength of the device. 33 2009-09-23
EBI, LLC 510(k) number 2009-04-02 Not classified Nonconforming Material/Component Some devices could have been made with raw material lots that may have inclusions, and could result in decreased strength of the device. 29 2009-09-23
EBI, LLC 510(k) number 2009-04-02 Not classified Nonconforming Material/Component Some devices could have been made with raw material lots that may have inclusions, and could result in decreased strength of the device. 44 2009-09-23
EBI, LLC 510(k) number 2009-03-27 Not classified Nonconforming Material/Component Certain lots of raw material contain inclusions that could potentially reduce the strength of some devices. 51 2009-09-23

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