Micro-Driver Minos

BUR, Long, Tapered Side-Cutting, Carbide FOR A211, A235 AND U211, 1.6 X 21.9 MM

Registry build 21.09.26
7manufacturers in China registered for this device type
40catalogue 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 Micro-Driver Minos
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 2021-06-29
Record revised 2024-08-14 (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

Catalogue Numbers

Catalogue numbers for Micro-Driver Minos
Catalogue number Size Status
X60R 6.0MM In distribution
L12T In distribution
L13S In distribution
M50R In distribution
L10D In distribution
M23R In distribution
M40D In distribution
L40R In distribution
M60R In distribution
L50R In distribution
X30D 3.0MM In distribution
X20R 2.0MM In distribution
L45C In distribution
M20T In distribution
M17S In distribution
L18R In distribution
M40R In distribution
X30R 3.0MM In distribution
L20T In distribution
X40B 4.0MM In distribution
M20D In distribution
X40D 4.0MM In distribution
X40R 4.0MM In distribution
M13S In distribution
M15S In distribution
X50D 5.0MM In distribution
X20D 2.0MM In distribution
L20D In distribution
M12T In distribution
L20R In distribution
X10D 1.0MM In distribution
M45C In distribution
L50D In distribution
M18R In distribution
L60R In distribution
X50R 5.0MM In distribution
L23R In distribution
M30R In distribution
M60D In distribution
L40D In distribution

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