Romeo 2 Instrumentation

Nav. Drill Sleeve

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
7510(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 Romeo 2 Instrumentation
Listed by Spineart SA, Switzerland
FDA product code OLO
Device type Orthopedic Stereotaxic Instrument
Device class Class 2
Regulation 21 CFR 882.4560
Establishment Specification developer, Complaint-file establishment, Manufacturer
Record published 2019-02-01
Record revised 2019-06-14 (version 3)

Specifications

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

Catalogue Numbers

Catalogue numbers for Romeo 2 Instrumentation
Catalogue number Size Status
NAV-IN 20 02-N 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
K261205 2026-07-29
K254158 2026-04-09
K242933 2025-06-18
K242890 2025-03-07
K241644 2024-08-07
K210472 2021-03-19
K183630 2019-06-10

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