Midas Rex Clearview™

Tool DC SD12MH25D LGD 12CM Dist 2.5 MH D

Registry build 21.09.26
2manufacturers in China registered for this device type
47catalogue numbers in this listing
8510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Shanghai (1), Guangdong (1).

Chinese manufacturers registered for FDA product code ERL
Manufacturer City Province Registered as Device types
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31
Guangdong Jinme Medical Technology Co., Ltd. Foshan Guangdong Manufacturer 13

Record

Regulatory record for Midas Rex Clearview™
Listed by Medtronic Xomed, Inc., United States
FDA product code ERL
Device type Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
Device class Class 2
Regulation 21 CFR 874.4250
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K081277
Record published 2016-07-22
Record revised 2018-07-06 (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
Sizes Length 12 to 14 cm; outer diameter 2 to 4 mm

Catalogue Numbers

Catalogue numbers for Midas Rex Clearview™
Catalogue number Size Status
SP14MH25 Length 14.0 cm In distribution
SD12MH25D In distribution
SP14MH25T In distribution
SP14MH30D Length 14.0 cm In distribution
SP12MH30T Length 12.0 cm In distribution
SP14BA30 In distribution
SP12BA40 Length 14.0 cm In distribution
SP14MH30T Length 14.0 cm In distribution
SD12MH25T In distribution
SP12MH25 Outer Diameter 2.5 mm In distribution
SP14MH30D In distribution
SP14MH25D In distribution
SD12MH30T Length 12.0 cm In distribution
SP12MH30D Outer Diameter 3.0 mm In distribution
SP12MH25T Length 12.0 cm In distribution
SP14BA30 Length 14.0 cm In distribution
SP14MH30T In distribution
SD12MH25 In distribution
SD12BA40 Outer Diameter 4.0 mm In distribution
SD12MH25T Length 12.0 cm In distribution
SD12MH30 In distribution
SP12BA40 In distribution
SP12MH25D Outer Diameter 2.5 mm In distribution
SD12MH30D Outer Diameter 3.0 mm In distribution
SP14MH30 In distribution
SP14MH30 Length 14.0 cm In distribution
SP12BA30 In distribution
SD12BA40 In distribution
SP14MH25D Length 14.0 cm In distribution
SP14BA40 In distribution
SP12MH25D In distribution
SP14BA40 Length 14.0 cm In distribution
SP12MH30 Length 12.0 cm In distribution
SP12MH30T In distribution
SP12BA30 Length 12.0 cm In distribution
SD12BA30 Outer Diameter 3.0 mm In distribution
SD12MH25D Outer Diameter 2.5 mm In distribution
SP12MH30 In distribution
SD12MH30D In distribution
SD12MH30 Outer Diameter 3.0 mm In distribution
SD12BA30 In distribution
SP12MH25 In distribution
SP12MH30D In distribution
SD12MH25 Length 12.0 cm In distribution
SP14MH25 In distribution
SP14MH25T Outer Diameter 2.5 mm In distribution
SP12MH25T In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ENT MR8 Medtronic Powered Surgical Solutions 234
Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece Anspach Effort, The 214
Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece Karl Storz GmbH & Co. KG 208
Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece Synthes Gmbh 126
Midas Rex Medtronic Powered Surgical Solutions 97
Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece Stryker GmbH 87
Midas REX Microsaws Medtronic Powered Surgical Solutions 75
Piezomed Pro Accessory W&H Dentalwerk Bürmoos GmbH 50
Zethon Zethon Ltd 39
NSK Sterile Burs/Drills Nakanishi Inc. 34
Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece Medtronic Xomed, Inc. 29
Core Stryker GmbH 27

Showing 12 of 169. All products under Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K150728 2015-08-14
K081277 2008-09-05
K073255 2008-03-24
K041523 2004-07-23
K041413 2004-07-12
K011321 2001-06-26
K002224 2000-12-04
K963246 1996-09-23

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Midas Rex Clearview™
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Medtronic Xomed, Inc. 510(k) number 2021-12-15 Class II Under Investigation by firm As a result of Medtronic’s integrated power console (authentication number: 222ACBZX00018000) being used with software version: v2.7.3.0, it was discovered that there was a defect that resulted in a difference between the set number of rota 1447 units 2023-06-09

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
2020-06-12 Class II Software design During internal testing execution of the next generation of Integrated Power Console (IPC) prototype it was noted that the M5 Microdebrider was rotating at a higher speed than the set value in the cosole. 673 units 2023-04-20
2009-07-17 Not classified Software design An error code (Code 13) is displayed on some of the consoles when a Medtronic Stylus or EHS handpiece is connected to the IPC indicating that the handpiece has not been recognized by the console. 493 2010-01-20

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