OS2®-V

OS2-V VARISATION STAPLE KIT, INTERAXIS 10 mm 26°

Registry build 21.09.26
7manufacturers in China registered for this device type
4catalogue numbers in this listing
1510(k) clearance
2recalls on this 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®-V
Listed by IN2BONES USA, LLC, United States
FDA product code JDR
Device type Staple, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K143323
Record published 2015-08-28
Record revised 2026-04-21 (version 9)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Special storage condition: KEEP DRY
Sizes Angle 26 to 90 °

Catalogue Numbers

Catalogue numbers for OS2®-V
Catalogue number Size Status
T10 SS260 Interaxis 10 mm In distribution
T10 SS908 Interaxis 8 mm In distribution
T10 SS268 Interaxis 8 mm In distribution
T10 SS900 Interaxis 10 mm In distribution

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
K161426 2016-10-24

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. 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
2026-05-11 Class II Process control Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label. 306 kits
2018-11-14 Class II Employee error The NeoSpan Compression Staple (10x10x10) kits from two lots contain the wrong size drill bit. They contain a 3mm drill bit instead of a 2mm drill bit. 30 units 2019-05-08

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