CannCompScrew 7.3mm (Classic)

CCScrew 7.3, L104, 32mm dis.thd.

Registry build 21.09.26
31manufacturers in China registered for this device type
33catalogue numbers in this listing
7510(k) clearances naming this product code
2recalls on this 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 CannCompScrew 7.3mm (Classic)
Listed by Trimed, Inc., 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
510(k) K093676
Record published 2016-09-07
Record revised 2025-02-06 (version 9)

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, manufacturing date

Catalogue Numbers

Catalogue numbers for CannCompScrew 7.3mm (Classic)
Catalogue number Size Status
CL7388 In distribution
C7344 In distribution
C7380 In distribution
C7354 In distribution
C7384 In distribution
C7376 In distribution
CL7360 In distribution
C7360 In distribution
CL73104 In distribution
CL7396 In distribution
CL7376 In distribution
C7368 In distribution
C7358 In distribution
CL7380 In distribution
CL7366 In distribution
CL7364 In distribution
CL73112 In distribution
CL7362 In distribution
C7350 In distribution
CL73100 In distribution
C7348 In distribution
CL7368 In distribution
CL7372 In distribution
C7372 In distribution
CL7392 In distribution
CL7384 In distribution
C7346 In distribution
C7356 In distribution
C7362 In distribution
CL73108 In distribution
C7352 In distribution
C7364 In distribution
C7388 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
K262344 2026-08-12
K261241 2026-05-14
K243943 2025-04-10
K234040 2024-01-18
K230749 2023-04-17
K211783 2021-08-06
K093676 2010-03-17

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
2024-03-19 Class II Process control Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque. 120 units
2024-03-19 Class II Process control Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque. 142 units

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