Diadust

DIADUST Micro Forceps, straight, 7 1/4", (185 mm), with plateau / platform tip, Golfball design handle, diamond dust coated, titanium, citrine, non-sterile, reusable

Registry build 21.09.26
99manufacturers in China registered for this device type
41catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Zhejiang (34), Jiangsu (25), Shanghai (9). 14 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HTD
Manufacturer City Province Registered as Device types
Shanghai Joy Crown Industry Co., Ltd. Pu Dong New Area Shanghai Contract manufacturer 64
Amsino Medical (Kunshan) Co., Ltd. Kunshan Jiangsu Contract manufacturer 53
Flexicare Medical (Dongguan) Ltd. Dongguan Guangdong Contract manufacturer 48
B.Braun Medical (Suzhou) Co,.Ltd Suzhou Jiangsu Contract manufacturer 37
Suzhou Microport Orthorecon Co., Ltd. Suzhou Jiangsu Contract manufacturer 31
Planet (Anhui) Medical Products Co., Ltd. Chuzhou Anhui Contract manufacturer 30
Jingmen Huasheng Asia Dynamics Sanitary Products Co., Ltd. Jingmen Hubei Contract manufacturer 23
Yiwu Haoding Medical Co., Ltd. Yiwu Zhejiang Contract manufacturer 23
Zhejiang Changdi Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 16
Linhai Deyi Plastic Co., Ltd. Linhai Zhejiang Contract manufacturer 15
Nantong City Yojo Medical Products Co., Ltd. Haimen Jiangsu Contract manufacturer 14
Meifu Medical Technology Suzhou Co., Ltd. Suzhou Jiangsu Contract manufacturer 13

Showing 12 of 99. All 99 manufacturers in China registered for Forceps

Record

Regulatory record for Diadust
Listed by Aesculap AG, Germany
FDA product code HTD
Device type Forceps
Device class Class 1
Regulation 21 CFR 878.4800
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2020-04-23
Record revised 2023-08-25 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Diadust
Catalogue number Size Status
BD200R In distribution
FM594R In distribution
FM327T In distribution
FM577R In distribution
FM574R In distribution
FM597R In distribution
BD192R In distribution
FM582R In distribution
FM585R In distribution
FM571R In distribution
FM586R In distribution
FM584R In distribution
FM575R In distribution
FD255R In distribution
FM318T In distribution
FM588R In distribution
BD196R In distribution
FD253R In distribution
FM579R In distribution
FM593R In distribution
BD194R In distribution
FM581R In distribution
BD193R In distribution
FM054R In distribution
FM328T In distribution
FM580R In distribution
FM595R In distribution
FM599R In distribution
FM587R In distribution
FM576R In distribution
FM573R In distribution
BD201R In distribution
FM317T In distribution
FM578R In distribution
FM589R In distribution
FM596R In distribution
FM583R In distribution
FM598R In distribution
FM572R In distribution
FM570R In distribution
FM329T In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Surgical Direct Surgical Direct, Inc. 1,186
Aesculap Aesculap AG 727
Wexler Surgical, Inc. Wexler Surgical, Inc. 636
HNM Medical HNM Stainless, LLC. 400
Millennium Avalign Technologies, Inc. 365
Forceps Synthes Gmbh 296
Princeton Princeton Medical Group, Inc. 271
MSI Precision Specialty Instruments MED Saver, Inc. 265
Ambler Surgical Ambler Surgical, LLC 212
Zoll-Dental Zoll-Dental 187
Forceps George Tiemann & Co. 184
Anmuth Medical International Anmuth Medical International LLC 174

Showing 12 of 963. All products under Forceps

Recalls

1 of these is 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
2025-01-31 Class II Use error The forceps have been used in ways not covered by the design resulting in breakage of the clamps. 93,714 forceps

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