Instrument, Surgical, Orthopedic, Ac-Powered Motor and Accessory/Attachment

Dyonics Powermax Elite Handpiece Hand-Controlled With Opposite-Side Suction Lever Refurbished

Registry build 21.09.26
23manufacturers in China registered for this device type
103catalogue numbers in this listing
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (8), Shanghai (6), Guangdong (3). 11 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HWE
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Microport Orthorecon Co., Ltd. Suzhou Jiangsu Contract manufacturer 31
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Autocam Medical Devices (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 9
Shaanxi Ansen Medical Technology Development Co., Ltd. Xi’An Shaanxi Contract manufacturer 7
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235

Showing 12 of 23. All 23 manufacturers in China registered for Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment

Record

Regulatory record for Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
Listed by Smith & Nephew, Inc., United States
FDA product code HWE
Device type Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
Device class Class 1
Regulation 21 CFR 878.4820
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2015-09-28
Record revised 2023-09-07 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date, serial number
Packaging Box of 6, box of 2
Distribution end date 2024-05-16

Catalogue Numbers

Catalogue numbers for Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
Catalogue number Size Status
210551 In distribution
3134182 In distribution
72204100 In distribution
3134180 In distribution
210554 In distribution
72204095 In distribution
3134192 In distribution
210550 In distribution
7207497 In distribution
E0014924-1 In distribution
7207496 In distribution
72200872F In distribution
210458 In distribution
3134191 In distribution
3134190 In distribution
3134189 In distribution
210447 In distribution
014425 In distribution
3134187 In distribution
6900854 In distribution
72204096 In distribution
3134033 In distribution
E0015067-1 In distribution
103044 In distribution
3134188 In distribution
3134183 In distribution
72200872SR In distribution
72200872 In distribution
72204111 In distribution
72202009 In distribution
72204099S In distribution
72204096S In distribution
E0014924-3 In distribution
72204111S In distribution
71110314 In distribution
72204112S In distribution
3134185 In distribution
72204094S In distribution
71935043 In distribution
210552 In distribution
7207492 In distribution
3134179 In distribution
7207315 In distribution
E0015067-2 In distribution
72204098S In distribution
E0014796-1 In distribution
72204097 In distribution
7207495 In distribution
7207493 In distribution
210455 In distribution
210454 In distribution
210449 In distribution
3134194 In distribution
210461 In distribution
72204104S In distribution
014485 In distribution
013666 In distribution
3134193 In distribution
7207498 In distribution
72204101S In distribution
72204091 In distribution
7207494 In distribution
72204102S In distribution
013549 In distribution
3134181 In distribution
3134186 In distribution
3134184 In distribution
E0015067-3 In distribution
72204112 In distribution
7210625 Withdrawn
7210624 Withdrawn
013543D Withdrawn
7210622 Withdrawn
13665 Withdrawn
014424 Withdrawn
013662D Withdrawn
014423 Withdrawn
014422 Withdrawn
13548 Withdrawn
7210621 Withdrawn
013550D Withdrawn
72204471 Withdrawn
014426 Withdrawn
013545D Withdrawn
13666 Withdrawn
E0014924-2 Withdrawn
2863 Withdrawn
7204890 Withdrawn
7210620 Withdrawn
014421 Withdrawn
013547D Withdrawn
72202479 Withdrawn
7205430 Withdrawn
013546D Withdrawn
210463 Withdrawn
7210623 Withdrawn
71935044 Withdrawn
71935262 Withdrawn
013664D Withdrawn
014432 Withdrawn
013499D Withdrawn
013666D Withdrawn
013661D Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
EZX Imedicom Co., Ltd. 441
Arthrex® Arthrex, Inc. 391
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment Stryker GmbH 284
Medicon Medicon eG. Chirurgiemechaniker-Genossenschaft 231
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment Synthes Gmbh 226
Brasseler EZX Imedicom Co., Ltd. 187
Conserve® Microport Orthopedics Inc. 158
R3 Smith & Nephew, Inc. 147
Trigen Smith & Nephew, Inc. 139
MicroPort Microport Orthopedics Inc. 134
Made-To-Order Tornier Inc. 131
Profemur® Microport Orthopedics Inc. 129

Showing 12 of 1,081. All products under Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment

Recalls

4 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
2015-09-10 Class II Package design/selection Sterility of device is compromised due to breach in the packaging 603 units 2021-06-23
2015-09-10 Class II Package design/selection Sterility of device is compromised due to breach in the packaging 1347 units 2021-06-23
2015-09-10 Class II Package design/selection Sterility of device is compromised due to breach in the packaging 1287 units 2021-06-23
2015-09-10 Class II Package design/selection Sterility of device is compromised due to breach in the packaging 1246 units 2021-06-23

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