Interventional Workspot
Software medical device hosting platform, used with a Philips Interventional X-Ray System. Provides common functionalities (e.g. import / export, data handling) for other software medical…
Software medical device hosting platform, used with a Philips Interventional X-Ray System. Provides common functionalities (e.g. import / export, data handling) for other software medical devices.
16manufacturers in China registered for this device type
1catalogue number
17510(k) clearances naming this product code
5recalls on this code
Who Else Makes It
Concentrated in Jiangsu (5), Shanghai (5), Beijing (3). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Shantou Institute OF Ultrasonic Instruments Co., Ltd. | Shantou | Guangdong | Contract manufacturer | 8 |
| iRay Imaging Technology (Haining) Limited | Haining | Zhejiang | Contract manufacturer | 6 |
| Chison Medical Technologies Co., Ltd. | Wuxi | Jiangsu | Contract manufacturer | 5 |
| Coretronic Projection (Kunshan) Corporation | Kunshan | Jiangsu | Contract manufacturer | 3 |
| Shenzhen Mindray BIO-Medical Electronics Co., Ltd. | Shenzhen | Guangdong | Specification developer | 61 |
| GE Medical Systems (China) Co., Ltd. | Wuxi | Jiangsu | Contract manufacturer | 57 |
| Arthrex (Shanghai) Co., Ltd. | Shanghai | Shanghai | Exporter | 38 |
| GE Hangwei Medical Systems Co., Ltd. | Beijing | Beijing | Specification developer | 22 |
| Shanghai United Imaging Healthcare Co., Ltd. | Shanghai | Shanghai | Manufacturer | 12 |
| Siemens Shanghai, Medical Equipment Ltd. | Shanghai | Shanghai | Contract manufacturer | 10 |
| Carestream Health, Inc., Global R&D Center | Shanghai | Shanghai | Specification developer | 8 |
| Beijing Infervision Healthcare Medical Technology Co., Ltd. | Beijing | Beijing | Complaint-file establishment | 4 |
Showing 12 of 16. All 16 manufacturers in China registered for System, Image Processing, Radiological
Record
| Listed by | Philips Medical Systems Nederland B.V., Netherlands |
|---|---|
| FDA product code | LLZ |
| Device type | System, Image Processing, Radiological |
| Device class | Class 2 |
| Regulation | 21 CFR 892.2050 |
| Establishment | Contract manufacturer, Remanufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter |
| Record published | 2016-09-24 |
| Record revised | 2025-12-15 (version 10) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Label carries | lot or batch number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| Interventional Workspot – 1 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Imagegrid Radiology Viewer System | Candelis, Inc. | 173 |
| Tims System | Foresight Imaging, LLC | 159 |
| System, Image Processing, Radiological | Biomet Microfixation | 146 |
| RamSoft | Ramsoft, Inc. | 65 |
| Joints | Medstrat | 62 |
| OrthoView | Meridian Technique Ltd | 54 |
| IPS | KLS-Martin L.P. | 48 |
| NovaPACS | Novarad Corp. | 42 |
| PointCloud Knee Instruments | Unik Orthopedics, Inc | 34 |
| DTX Studio™ Clinic | Nobel Biocare AB | 34 |
| Eaglesoft | Patterson Technology Center | 33 |
| Medtronic Navigation | Medtronic Navigation, Inc. | 26 |
Showing 12 of 1,109. All products under System, Image Processing, Radiological
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K251215 | 2025-10-02 |
| K250181 | 2025-07-15 |
| K242512 | 2024-10-24 |
| K221270 | 2022-05-31 |
| K201573 | 2021-08-17 |
| K200713 | 2020-04-09 |
| K181177 | 2018-05-31 |
| K173467 | 2017-12-12 |
| K163250 | 2017-05-11 |
| K162484 | 2017-02-23 |
| K162955 | 2016-12-19 |
| K160315 | 2016-02-19 |
| K130278 | 2013-05-29 |
| K121296 | 2013-01-02 |
| K121781 | 2012-10-26 |
| K111245 | 2011-07-29 |
| K083740 | 2009-02-13 |
Recalls Naming This Product
9 recalls name this product by its own identifiers, the UDI on its label.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Philips Medical Systems Nederland B.V. | UDI-DI | 2025-01-13 | Class II | Device Design | Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longit | 474 units US; 1908 units OUS | |
| Philips Medical Systems Nederland B.V. | UDI-DI | 2025-01-13 | Class II | Device Design | Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longit | 146 units US; 629 units OUS | |
| Philips Medical Systems Nederland B.V. | UDI-DI | 2024-01-02 | Class II | Process design | Framegrabber card may not perform as intended. Monitor may show no viewports, or show one or more viewports may show no image, a distorted image, or a frozen image. Switching between viewports on the monitor may not be possible. Issue may r | 1,993 US; 2,662 OUS | |
| Philips Medical Systems Nederland B.V. | UDI-DI | 2024-01-02 | Class II | Process design | Framegrabber card may not perform as intended. Monitor may show no viewports, or show one or more viewports may show no image, a distorted image, or a frozen image. Switching between viewports on the monitor may not be possible. Issue may r | 1,993 US; 2,662 ROW | |
| Philips Medical Systems Nederland B.V. | UDI-DI | 2024-01-02 | Class II | Process design | Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure. | 13, 133 (3,408 US; 9,725 ROW) | |
| Philips Medical Systems Nederland B.V. | UDI-DI | 2024-01-02 | Class II | Process design | Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure. | 13, 133 (3,408 US; 9,725 ROW) | |
| Philips Medical Systems Nederland B.V. | UDI-DI | 2024-01-02 | Class II | Process design | Dual In-Line Memory Modules (DIMMs) may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure. | 5,500 (1,681 US; 3,819 ROW) | |
| Philips Medical Systems Nederland B.V. | UDI-DI | 2023-06-12 | Class II | Component design/selection | The bolts supporting the FlexMove Carriage may become loose and/or break, and cracks may appear in the suspension rail of the FlexMove Carriage. | 648 units | |
| Philips North America LLC | UDI-DI | 2021-11-19 | Class II | Other | Set screws securing the two gliding rods of the Extra Monitors (called 7th and 8th monitor) mounted on the Monitor Ceiling Suspension (MCS) can come loose, the Extra monitors might disengage from the Mounting Ceiling Suspension structure an | USA: 5 systems R.O.W.: 15 systems | 2024-02-07 |
Recalls
5 of these are 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.
| Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|
| 2026-03-19 | Class II | Labeling design | Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA) ratio of AneurysmFlow (Interventional Tool). Philips has determined that the MAFA ratio does not provide reliable prognostic information regarding aneurysm occlusion f | 1,033 units |
| 2026-03-05 | Class II | Software design | Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence. | 3,552 units |
| 2025-08-08 | Class II | Software design | Software issue that results in the display of outdated information. | 4 units |
| 2025-04-07 | Class II | Software in the Use Environment | An issue was identified with the software when using the Echo Module of ISCV, the issue may result in missing or incomplete information in the report. | 996 units (267 US, 729 OUS) |
| 2024-04-04 | Class II | Software design | Study data is not able to be archived, copied, or exported with the cardiovascular software version. | 139 |
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.