Vortex Surgical Inc

25ga Kit (ILM Forceps, Retractable Edge Advantage, Soft Tip) Box of 5

Registry build 21.09.26
67manufacturers in China registered for this device type
13catalogue numbers in this listing
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (26), Shanghai (11), Zhejiang (9). 12 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KDD
Manufacturer City Province Registered as Device types
Hangzhou Rollmed Co., Ltd. Hangzhou Zhejiang Contract manufacturer 127
Gcmedica Enterprise Ltd.(Wuxi) Wuxi Jiangsu Contract manufacturer 55
Allmed Medical Products Co., Ltd. Zhijiang Hubei Contract manufacturer 43
Conod Medical Shuyang Co., Ltd. Shuyang Jiangsu Contract manufacturer 22
Primecare Medical (Suzhou) Co., Ltd. Changshu Jiangsu Contract manufacturer 20
Exact Medical Manufacturing, Inc. Changzhou Jiangsu Contract manufacturer 17
Beilun Plastech Inc Ningbo Zhejiang Contract manufacturer 13
Meifu Medical Technology Suzhou Co., Ltd. Suzhou Jiangsu Contract manufacturer 13
Winner Medical (Chongyang) Co., Ltd. Chongyang Hubei Contract manufacturer 13
Wenzhou Baiyu Glasses Technology Co., Ltd. Wenzhou Zhejiang Contract manufacturer 10
Jiangsu Xuhe Medical Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 9
Nanjing HI-Tech Tape Products Co., Ltd. Nanjing Jiangsu Contract manufacturer 8

Showing 12 of 67. All 67 manufacturers in China registered for Kit, Surgical Instrument, Disposable

Record

Regulatory record for Vortex Surgical Inc
Listed by Vortex Surgical, Inc., United States
FDA product code KDD
Device type Kit, Surgical Instrument, Disposable
Device class Class 1
Regulation 21 CFR 878.4800
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2023-02-02

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Vortex Surgical Inc
Catalogue number Size Per pack Status
VS0500 10 In distribution
VS0640.23-XEX 5 In distribution
VS0640.23-FEX 5 In distribution
VS0640.23-XXS 5 In distribution
VS0644.25-FXX 5 In distribution
VS0640.25-FEX 5 In distribution
VS0640.25-XEX 5 In distribution
VS0640.23-XES 5 In distribution
VS0510 10 In distribution
VS0520 10 In distribution
VS0640.25-XXS 5 In distribution
VS0644.25-XES 5 In distribution
VS0640.25-XES 5 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Medline Industries, Inc. Medline Industries, Inc. 789
CustomEyes® Beaver-Visitec International, Ltd 696
DeRoyal Deroyal Industries, Inc. 589
Centurion Centurion Medical Products Corporation 277
Readypak Kit Beaver-Visitec International, Ltd 196
Custom Healthcare Systems, Inc. Manus Medical, LLC 78
Medical Action Industries Medical Action Industries, Inc. 76
Bioseal Inc. Bioseal 38
A. Titan Instruments A. Titan Instruments, Inc. 37
In2Bones IN2BONES USA, LLC 24
Aero-Med Aero-MED LLC 23
Medline Medline Industries, Inc. 17

Showing 12 of 252. All products under Kit, Surgical Instrument, Disposable

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
2025-12-16 Class II Employee error There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection. 14,789 (8651 US; 6138 OUS)
2025-12-16 Class II Employee error There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection. 14,789 (8651 US; 6138 OUS)

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