Lantern Surgical Assistant (LSA)
Packaged Assembly, Navigation Unit, LSA Knee
5manufacturers in China registered for this device type
15catalogue numbers in this listing
12510(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.
| 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
| Listed by | OrthAlign, Inc., United States |
|---|---|
| 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 |
| 510(k) | K200892 |
| Record published | 2023-01-31 |
| Record revised | 2025-11-17 (version 4) |
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 |
| Latex | Labelled latex-free |
| Label carries | lot or batch number, expiry date, serial number |
| Storage | Storage environment temperature -22 to 140 °F; Handling environment temperature -22 to 140 °F |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 402505 | In distribution | |
| 405185-01 | In distribution | |
| 402474 | In distribution | |
| 406001-01 | In distribution | |
| KA406000-02 | In distribution | |
| 406000-02-CE | In distribution | |
| 401785 | In distribution | |
| 402477 | In distribution | |
| 402472 | In distribution | |
| 402473 | In distribution | |
| 405204-KA | In distribution | |
| 406000-01 | In distribution | |
| 402475 | In distribution | |
| 401788 | In distribution | |
| 406000-02 | In distribution |
Same 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
| Clearance | Decision date |
|---|---|
| K200892 | 2020-06-18 |
| K200642 | 2020-04-10 |
| K172462 | 2017-11-22 |
| K171780 | 2017-07-11 |
| K163379 | 2017-03-02 |
| K162962 | 2017-01-23 |
| K153237 | 2016-03-01 |
| K140331 | 2014-06-10 |
| K130387 | 2013-11-08 |
| K103829 | 2011-04-04 |
| K093998 | 2010-03-22 |
| K091411 | 2009-09-25 |
Recalls Naming This Product
2 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| OrthAlign, Inc. | 510(k) number | 2026-02-10 | Class II | Nonconforming Material/Component | Drill plates manufactured out of specification can result in a bone cut in excess 00800″(2.8448mm) | 7 units |
| OrthAlign, Inc. | 510(k) number | 2026-02-10 | Class II | Nonconforming Material/Component | Drill plates manufactured out of specification can result in a bone cut in excess 00800″(2.8448mm) | 7 units |
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.