Remi Robotic Navigation System

REMI 6.5 mm Cann. Dual Lead Tap

Registry build 21.09.26
5manufacturers in China registered for this device type
27catalogue numbers in this listing
2510(k) clearances naming this product 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 Remi Robotic Navigation System
Listed by Fusion Robotics, LLC, United States
FDA product code OLO
Device type Orthopedic Stereotaxic Instrument
Device class Class 2
Regulation 21 CFR 882.4560
Record published 2023-03-20
Record revised 2026-04-01 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, serial number
Distribution end date 2026-03-31

Catalogue Numbers

Catalogue numbers for Remi Robotic Navigation System
Catalogue number Size Status
1365 Withdrawn
1345 Withdrawn
1355 Withdrawn
1050 Withdrawn
1385 Withdrawn
1066 Withdrawn
5005 Withdrawn
1025 Withdrawn
6025 Withdrawn
1035 Withdrawn
1375 Withdrawn
1045 Withdrawn
6026 Withdrawn
1026 Withdrawn
1102 Withdrawn
1061 Withdrawn
PN-001 Withdrawn
3007 Withdrawn
1065 Withdrawn
1015 Withdrawn
1010 Withdrawn
1005 Withdrawn
1350 Withdrawn
3005 Withdrawn
1030 Withdrawn
1060 Withdrawn
1040 Withdrawn

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
K223350 2023-03-13
K223070 2022-10-28

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