Aim™dynamic Tibial Nail

70 catalogue numbers from 8105-10-300, 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
70catalogue 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 Aim™dynamic Tibial Nail
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) K972183
Record published 2015-10-24
Record revised 2025-05-30 (version 4)

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

Catalogue Numbers

Catalogue numbers for Aim™dynamic Tibial Nail
Catalogue number Size Status
8105-10-300 10MM X 30CM In distribution
8105-09-300 9MM X 30CM In distribution
8105-08-270 8MM X 27CM In distribution
8105-09-315 9MM X 31.5CM In distribution
8105-10-390 10MM X 39CM In distribution
8105-12-360 12MM X 36CM In distribution
8105-08-330 8MM X 33CM In distribution
8105-12-315 12MM X 31.5CM In distribution
8105-11-255 11MM X 25.5CM In distribution
8105-13-345 13MM X 34.5CM In distribution
8105-08-300 8MM X 30CM In distribution
8105-08-405 8MM X 40.5CM In distribution
8105-12-390 12MM X 39CM In distribution
8105-09-405 9MM X 40.5CM In distribution
8105-11-360 11MM X 36CM In distribution
8105-10-345 10MM X 34.5CM In distribution
8105-09-255 9MM X 25.5CM In distribution
8105-09-420 9MM X 42CM In distribution
8105-10-360 10MM X 36CM In distribution
8105-10-255 10MM X 25.5CM In distribution
8105-11-300 11MM X 30CM In distribution
8105-11-285 11MM X 28.5CM In distribution
8105-09-285 9MM X 28.5CM In distribution
8105-12-405 12MM X 40.5CM In distribution
8105-10-285 10MM X 28.5CM In distribution
8105-13-360 13MM X 36CM In distribution
8105-11-270 11MM X 27CM In distribution
8105-08-345 8MM X 34.5CM In distribution
8105-10-330 10MM X 33CM In distribution
8105-09-270 9MM X 27CM In distribution
8105-12-420 12MM X 42CM In distribution
8105-12-345 12MM X 34.5CM In distribution
8105-11-345 11MM X 34.5CM In distribution
8105-12-270 12MM X 27CM In distribution
8105-13-285 13MM X 28.5CM In distribution
8105-11-420 11MM X 42CM In distribution
8105-08-375 8MM X 37.5CM In distribution
8105-08-315 8MM X 31.5CM In distribution
8105-13-315 13MM X 31.5CM In distribution
8105-10-375 10MM X 37.5CM In distribution
8105-12-285 12MM X 28.5CM In distribution
8105-12-375 12MM X 37.5CM In distribution
8105-09-330 9MM X 33CM In distribution
8105-13-255 13MM X 25.5CM In distribution
8105-11-330 11MM X 33CM In distribution
8105-11-390 11MM X 39CM In distribution
8105-10-420 10MM X 42CM In distribution
8105-13-330 13MM X 33CM In distribution
8105-13-300 13MM X 30CM In distribution
8105-12-330 12MM X 33CM In distribution
8105-09-390 9MM X 39CM In distribution
8105-08-360 8MM X 36CM In distribution
8105-13-375 13MM X 37.5CM In distribution
8105-11-375 11MM X 37.5CM In distribution
8105-09-345 9MM X 34.5CM In distribution
8105-08-285 8MM X 28.5CM In distribution
8105-13-420 13MM X 42CM In distribution
8105-08-255 8MM X 25.5CM In distribution
8105-09-360 9MM X 36CM In distribution
8105-10-270 10MM X 27CM In distribution
8105-08-390 8MM X 39CM In distribution
8105-11-405 11MM X 40.5CM In distribution
8105-13-390 13MM X 39CM In distribution
8105-08-420 8MM X 42CM In distribution
8105-09-375 9MM X 37.5CM In distribution
8105-10-405 10MM X 40.5CM In distribution
8105-11-315 11MM X 31.5CM In distribution
8105-10-315 10MM X 31.5CM In distribution
8105-13-405 13MM X 40.5CM In distribution
8105-12-300 12MM X 30CM 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

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

Recalls naming the identifiers of Aim™dynamic Tibial Nail
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet, Inc. 510(k) number 2018-02-06 Class II Under Investigation by firm The AIM Tibial Nails failed a clinical analysis where the surgical revision rate exceeded the acceptance criteria in the Device Performance Review protocol for the implant system. Not known 2019-04-02
Biomet, Inc. 510(k) number 2018-02-06 Class II Under Investigation by firm The AIM Tibial Nails failed a clinical analysis where the surgical revision rate exceeded the acceptance criteria in the Device Performance Review protocol for the implant system. Not known 2019-04-02

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