E9000

6.5 X 38mm E9000 Fluted Low Speed Optimum Bur, Round, Carbide

Registry build 21.09.26
7manufacturers in China registered for this device type
53catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (2), Shandong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code GFF
Manufacturer City Province Registered as Device types
Aplus (Guangzhou) Medical Technology Company Guangzhou Guangdong Contract manufacturer 6
Xinhua Surgical Instrument Co., Ltd. Zibo Shandong Manufacturer 222
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Shanghai Wilpower Industrial Co., Ltd. Shanghai Shanghai Exporter 33
Jiangsu Huadong Medical Device Industry Co., Ltd. Yangzhou Jiangsu Contract manufacturer 29
Zonefly Medical Devices Co., Ltd. Danyang Jiangsu Specification developer 7
Jiangxi Vision Plus Medical Technology Co., Ltd. Nanchang Jiangxi Manufacturer 6

Record

Regulatory record for E9000
Listed by ConMed Corporation, United States
FDA product code GFF
Device type Bur, Surgical, General & Plastic Surgery
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 2021-10-14
Record revised 2024-08-01 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Sizes Outer diameter 0.7 to 3 mm; length 25 mm
Distribution end date 2024-06-07

Catalogue Numbers

Catalogue numbers for E9000
Catalogue number Size Status
E5160 In distribution
E8020 In distribution
E6160 In distribution
E8030LSO In distribution
E6150 In distribution
00702196000 Outer Diameter 3 mm In distribution
E8230LSO In distribution
E6040 In distribution
E8110 In distribution
E8205 In distribution
E8150LSO In distribution
E6250 In distribution
E8240LSO In distribution
E5140 In distribution
E8210 In distribution
E6240 In distribution
E8025 In distribution
E8010 In distribution
E6210 In distribution
E8015 In distribution
E6115 In distribution
E8040LSO In distribution
E6205 In distribution
E6130 In distribution
E6215 In distribution
E6120 In distribution
E8050LSO In distribution
E8120 In distribution
E5220 In distribution
E5210 In distribution
E8250LSO In distribution
E6110 In distribution
E5170 In distribution
E6220 In distribution
E8207 In distribution
E5240 In distribution
E5050 In distribution
E6125 Outer Diameter 2.5 mm In distribution
E8130LSO In distribution
E8140LSO In distribution
E6230 In distribution
E8215 In distribution
E8225 In distribution
E4115 In distribution
E6140 In distribution
E5130 In distribution
E5230 In distribution
E6207 Outer Diameter 0.7 mm In distribution
E5215 In distribution
E8165LSO In distribution
E8065LSO In distribution
E8220 In distribution
E5225 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Komet Surgical Bur Gebr. Brasseler Gmbh & Co. KG 1,011
Bur, Surgical, General & Plastic Surgery Sterilmed, Inc. 1,001
Medline Medline Industries, Inc. 584
Brasseler USA Peter Brasseler Holdings, LLC 335
Bur, Surgical, General & Plastic Surgery Omega Surgical Instruments, Inc. 312
Bur, Surgical, General & Plastic Surgery Hager & Meisinger Gesellschaft mit beschränkter Haftung 170
MicroAire® Microaire Surgical Instruments LLC 162
Ultrapower ConMed Corporation 155
De Soutter Medical DE Soutter Medical Ltd. 143
Jota Jota AG 112
Conmed ConMed Corporation 109
Bur, Round, round shank Gebr. Brasseler Gmbh & Co. KG 104

Showing 12 of 167. All products under Bur, Surgical, General & Plastic Surgery

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 Closed
2015-12-21 Class II Mixed-up of materials/components Metal shavings released from burs during use are due to contact between the bur and the hood of the PreBent Bur assembly. During the manufacturing process an assembly error occurred which caused inadvertent mixing of two sizes of bearings. 991 pieces 2018-05-24

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