Aesculap

HI-Line XXS Disp.diamond Burr III D5.0MM

Registry build 21.09.26
7manufacturers in China registered for this device type
72catalogue numbers in this listing
1510(k) clearance
3recalls on this code

Who Else Makes It

Concentrated in Guangdong (5), Zhejiang (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GEY
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Shenzhen Jinlichang Electronic Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 1
Dongguan Wanjin Industrial Co., Ltd. Dongguang Guangdong Remanufacturer 41
Guangzhou Ajax Medical Equipment Co Ltd Guangzhou Guangdong Manufacturer 13
Shenzhen Soga Technology Co., Ltd. Shenzhen Guangdong Manufacturer 7
Ningbo Advan Electrical Co., Ltd. Cixi Zhejiang Contract manufacturer 5

Record

Regulatory record for Aesculap
Listed by Aesculap AG, Germany
FDA product code GEY
Device type Motor, Surgical Instrument, Ac-Powered
Device class Class 1
Regulation 21 CFR 878.4820
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2020-04-24
Record revised 2021-05-07 (version 5)

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
Label carries lot or batch number, expiry date, serial number
Distribution end date 2026-05-29
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Aesculap
Catalogue number Size Per pack Status
GB551SU In distribution
GD051R In distribution
GD394R 5 In distribution
GE848SU In distribution
GC925R In distribution
GD047R In distribution
GD390R 5 In distribution
GA263SU In distribution
GD392R 5 In distribution
GA261SU In distribution
GB695R In distribution
GD152R In distribution
GC926R In distribution
GD255R In distribution
GD132R In distribution
GD145R In distribution
GE835SU In distribution
GC380R In distribution
GD393R 5 In distribution
GD391R 5 In distribution
GC314R In distribution
GD397R 5 In distribution
GD035R In distribution
GD225R In distribution
GD082R In distribution
GD135R In distribution
GD071R In distribution
GC880R In distribution
GB696R In distribution
GD396R 5 In distribution
GE818SU In distribution
GA264SU In distribution
GD062R In distribution
GE805SU In distribution
GA223R In distribution
GA258SU In distribution
GD024R In distribution
GD072R In distribution
GD951R 5 In distribution
GD231R In distribution
GB693 10 In distribution
GD248R In distribution
GE842SU In distribution
GD085R In distribution
GC378R In distribution
GD034R In distribution
GD073R In distribution
GD250R In distribution
GD151R In distribution
GA259SU In distribution
GD232R In distribution
GA262SU In distribution
GD395R 5 In distribution
GA156 In distribution
GD230R In distribution
GD044R In distribution
GD063R In distribution
GD950R 5 In distribution
GD247R In distribution
GD033R In distribution
GD227R In distribution
GC644R Withdrawn
GP494R 5 Withdrawn
GC491R Withdrawn
GA222R Withdrawn
GP545R 5 Withdrawn
GP544R 5 Withdrawn
GA228R Withdrawn
GE812SU Withdrawn
GP497R 5 Withdrawn
GA227R Withdrawn
GA221R Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
De Soutter Medical DE Soutter Medical Ltd. 1,481
HI-Line XS Aesculap AG 169
Zaguar Imedicom Co., Ltd. 131
Elan 4 Aesculap AG 107
HI-Line Aesculap AG 53
Motor, Surgical Instrument, Ac-Powered Anspach Effort, The 37
Zimmer Biomet™ Zimmer Surgical, Inc. 29
Motor, Surgical Instrument, Ac-Powered Synthes Gmbh 29
HI-Line XXS Aesculap AG 22
Motor, Surgical Instrument, Ac-Powered Smith & Nephew, Inc. 20
Eccos Aesculap AG 11
Motor, Surgical Instrument, Ac-Powered Richard Wolf Gmbh 10

Showing 12 of 149. All products under Motor, Surgical Instrument, Ac-Powered

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K913262 1991-12-30

Recalls

3 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
2017-03-28 Class II Process control Diamond particulates may break off the burr and fall into the surgical site. If the particles are not detected and are not removed from the surgical site a foreign body reaction may occur. These particulates could also lead to mechanically total amount of burrs – 608 2018-02-06
2017-03-28 Class II Process control Diamond particulates may break off the burr and fall into the surgical site. If the particles are not detected and are not removed from the surgical site a foreign body reaction may occur. These particulates could also lead to mechanically total of all burrs 608 units 2018-02-06
2017-03-28 Class II Process control Diamond particulates may break off the burr and fall into the surgical site. If the particles are not detected and are not removed from the surgical site a foreign body reaction may occur. These particulates could also lead to mechanically Total of all burrs – 608 units 2018-02-06

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