Volt™ Wrist Treatment System

2.7mm Cannulated Locking Screw T8/12mm

Registry build 21.09.26
31manufacturers in China registered for this device type
40catalogue numbers in this listing
9510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (15), Shanghai (5), Zhejiang (3). 19 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HWC
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
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
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11

Showing 12 of 31. All 31 manufacturers in China registered for Screw, Fixation, Bone

Record

Regulatory record for Volt™ Wrist Treatment System
Listed by Tyber Medical, United States
FDA product code HWC
Device type Screw, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2025-10-21

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Volt™ Wrist Treatment System
Catalogue number Size Status
02.527.512 In distribution
02.527.522 In distribution
02.527.422 In distribution
02.527.412TS In distribution
02.527.418 In distribution
02.527.524TS In distribution
02.527.424 In distribution
02.527.524 In distribution
02.527.416TS In distribution
02.527.530 In distribution
02.527.414 In distribution
02.527.414TS In distribution
02.527.514 In distribution
02.527.512TS In distribution
02.527.518TS In distribution
02.527.416 In distribution
02.527.426TS In distribution
02.527.530TS In distribution
02.527.520 In distribution
02.527.520TS In distribution
02.527.410 In distribution
02.527.510TS In distribution
02.527.516TS In distribution
02.527.510 In distribution
02.527.410TS In distribution
02.527.514TS In distribution
02.527.522TS In distribution
02.527.526 In distribution
02.527.412 In distribution
02.527.426 In distribution
02.527.422TS In distribution
02.527.420 In distribution
02.527.424TS In distribution
02.527.516 In distribution
02.527.518 In distribution
02.527.528 In distribution
02.527.418TS In distribution
02.527.526TS In distribution
02.527.420TS In distribution
02.527.528TS In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Screw, Fixation, Bone Synthes Gmbh 3,975
Aptus Medartis Inc. 3,623
Acumed Acumed LLC 3,187
Arthrex® Arthrex, Inc. 2,781
OsteoMed Osteomed 2,764
Screw, Fixation, Bone AAP Implantate AG 2,176
Screw, Fixation, Bone Zimmer, Inc. 1,993
Arix System Bone Screw Jeil Medical Corporation 1,875
Cannulated Screw System + Tyber Medical 1,814
Cannulated Compression Headless Screw Tyber Medical 1,621
Microware Bone Plates and Bone Screws Microware Precision Co., Ltd. 1,601
Anthem Globus Medical, Inc. 1,538

Showing 12 of 5,775. All products under Screw, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253042 2026-04-03
K252901 2025-12-31
K192975 2020-01-09
K192974 2020-01-08
K170571 2017-06-20
K161597 2016-11-16
K153575 2016-02-26
K153180 2015-11-25
K133842 2014-03-20

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