Excelsiusflex

ExcelsiusFlex is a robotic positioning system with a computer-controlled robotic arm, hardware and software that works with ExcelsiusHub. The FDA filing describes it as providing real-time…

Registry build 21.09.26

ExcelsiusFlex is a robotic positioning system with a computer-controlled robotic arm, hardware and software that works with ExcelsiusHub. The FDA filing describes it as providing real-time surgical navigation and robotic guidance using patient-tracking arrays and a positioning camera.

For knee procedures, the system assists with planning femoral and tibial implant positions and preparing bone during total knee arthroplasty. The filing says it constrains the robotic arm to planned resection planes based on plans developed before or during surgery.

Listed Item

Sawblade Calibration Attachment, EFlex

Device Function and Design

The FDA summary also describes locating anatomical structures and positioning a tool holder for compatible surgical instruments. It says the system helps plan implant positions and prepare bone during orthopedic procedures.

5manufacturers in China registered for this device type
20catalogue numbers in this listing
13510(k) clearances naming this product code
2recalls 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 Excelsiusflex
Listed by Globus Medical, Inc., United States
FDA product code OLO
Device type Orthopedic Stereotaxic Instrument
Device class Class 2
Regulation 21 CFR 882.4560
Establishment Manufacturer, Exporter
510(k) K240721
Record published 2024-12-17
Record revised 2026-03-19 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Label carries lot or batch number, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Excelsiusflex
Catalogue number Size Status
6221.2612 In distribution
6258.1001 In distribution
6221.2602 In distribution
6221.2503 In distribution
6221.2712 In distribution
6221.2615 In distribution
6221.2684 In distribution
6221.2614 In distribution
6221.2608 In distribution
6221.2601 In distribution
6221.2505 In distribution
6221.2607 In distribution
6221.2716 In distribution
6221.2713 In distribution
6221.2616 In distribution
6221.2714 In distribution
6221.2715 In distribution
6221.2617 In distribution
6221.2717 In distribution
6221.2613 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
K250599 2025-11-05
K243814 2025-01-10
K243671 2024-12-20
K240721 2024-06-14
K240568 2024-04-29
K233638 2024-02-09
K211616 2021-08-25
K200047 2020-07-10
K191100 2019-07-24
K190653 2019-04-09
K180690 2018-06-25
K171651 2017-08-16
K153203 2016-02-03

Recalls

1 of these is Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. 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
2023-12-15 Class II Device Design Devices may not be rendered sterile due to an internal gap that may be present on some devices causing increased difficulty cleaning prior to steam sterilization. There is an increased risk for infection, inflammation, local toxicity, syste 570
2023-12-07 Class I Device Design A calibration error associated with the Flat Panel Fluoroscopy Fixture when used with ExcelsiusGPS for fluoroscopy workflow may lead to inaccurate navigation, which may result in device misplacement. 9

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