Long Drill Guide

4 catalogue numbers from MAS2242-07S, listed by Mazor Robotics Ltd., Israel, under Orthopedic Stereotaxic Instrument. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
4catalogue numbers in this listing
10510(k) clearances naming this product code
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (2), Shanghai (1), Guangdong (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OLO
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
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for Long Drill Guide
Listed by Mazor Robotics Ltd., Israel
FDA product code OLO
Device type Orthopedic Stereotaxic Instrument
Device class Class 2
Regulation 21 CFR 882.4560
Establishment Specification developer, Manufacturer
510(k) K230064
Record published 2024-03-14
Record revised 2026-05-07 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied as a kit Yes
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Long Drill Guide
Catalogue number Size Status
MAS2242-07S In distribution
MAS2242-06S In distribution
MAS2242-04 In distribution
MAS2242-05S In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Valence Robotic Navigation System Alphatec Spine, Inc. 813
Olympic Astura Medical 684
Excelsius GPS Globus Medical, Inc. 383
Orthopedic Stereotaxic Instrument Medtronic Navigation, Inc. 356
Masada Astura Medical 335
Excelsiusgps Globus Medical, Inc. 297
Invictus Alphatec Spine, Inc. 235
OrthAlign Plus OrthAlign, Inc. 210
Arvis ® Kico Knee Innovation Company 174
OMNIBotics Omni Life Science, Inc. 150
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 137
Navigation Instruments VB Spine LLC 135

Showing 12 of 1,127. All products under Orthopedic Stereotaxic Instrument

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K251316 2025-09-11
K230064 2023-04-07
K203005 2020-10-27
K200935 2020-05-08
K182077 2018-11-02
K180307 2018-04-30
K172522 2017-09-15
K163221 2017-04-04
K152041 2015-11-17
K140167 2014-09-10

Recalls Naming This Product

3 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Long Drill Guide
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Mazor Robotics Ltd. 510(k) number 2025-12-10 Class II Under Investigation by firm Software errors that can result in incorrect surgical instrument positioning during spinal surgery. 549 systems
Mazor Robotics Ltd. 510(k) number 2024-07-17 Class II Device Design Software anomalies which can result in two separate issues: A lagging screen display during a navigated procedure; or the potential for a mismatch between the navigated screw and the screw information presented on the screen. 94 devices
Mazor Robotics Ltd. 510(k) number 2023-09-05 Class II Software design Software update 324 devices

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
2019-07-02 Class II Other The firm has become aware that the Snapshot Trackers were not manufactured in accordance with specifications and could potentially lead to navigational inaccuracies, which may result in patient injury, e.g. nerve damage or neurological def 93 snapshot trackers 2022-02-02

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