OS2®-C

OS2-C is a compression staple for fixation of arthrodeses, osteotomies and fractures in hand or foot surgery. It is designed to maintain compression across the treated bone site. The…

Registry build 21.09.26

OS2-C is a compression staple for fixation of arthrodeses, osteotomies and fractures in hand or foot surgery. It is designed to maintain compression across the treated bone site.

The implant is made from uncoated PEEK-Optima and supplied gamma-sterilized, preassembled on an inserter. Different leg lengths and interaxis dimensions, from 11 to 15 mm, support selection for the procedure.

Surgical Use

The staple is intended for one use in a hospital or outpatient surgery center where a sterile field can be maintained. The number and size of staples are adapted to the indication and fixation requirements.

7manufacturers in China registered for this device type
3catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (2), Guangdong (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JDR
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Kingj Medical Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Hangzhou Sino-MIM Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38

Record

Regulatory record for OS2®-C
Listed by In2Bones SAS, France
FDA product code JDR
Device type Staple, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Specification developer, Manufacturer, Exporter
510(k) K153395
Record published 2016-03-23
Record revised 2025-12-15 (version 8)

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
Distribution end date 2024-12-27

Catalogue Numbers

Catalogue numbers for OS2®-C
Catalogue number Size Status
T30 SP150 Interaxis 15mm Withdrawn
T30 SP110 Interaxis 11mm Withdrawn
T30 SP130 Interaxis 13mm Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DynaBridge Fusion Orthopedics, LLC 156
Arthrex® Arthrex, Inc. 80
Staple, Fixation, Bone Smith & Nephew, Inc. 59
Compression Staple System Tornier Inc. 36
UNI-Clip Newdeal Sas 35
Z-Staple Z-Medical Gmbh & Co. KG 34
Orbitum Staple System CPM Medical Consultants, LLC. 32
OSStaple Biomedical Enterprises, Inc. 30
Acumed Acumed LLC 30
Stealthfix Intraosseous Fixation System Medartis Inc. 29
Staple, Fixation, Bone Stryker GmbH 29
Step Boss Biomedical Enterprises, Inc. 27

Showing 12 of 319. All products under Staple, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K153770 2016-03-21
K153395 2016-02-18
K143323 2015-02-26

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