Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Philips. FDA records under 5 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Philips Medical Systems DMC GmbH with 44 device recalls, 19 510(k) clearances and 1 AI-enabled device. The most recent is a device recall dated Oct 1, 2025: Radiography 7300 C; Model Number: 712037;.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Oct 1, 2025 | Radiography 7300 C; Model Number: 712037;Class II · Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 | Device recalls |
| Oct 1, 2025 | DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;Class II · Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 | Device recalls |
| Oct 1, 2025 | Precision CRF; Model Number: 706400;Class II · Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 | Device recalls |
| Oct 1, 2025 | ProxiDiagnost N90; Model Number: 706110;Class II · Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 | Device recalls |
| Oct 1, 2025 | CombiDiagnost R90; Model Number: 709031;Class II · Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 | Device recalls |
| Oct 1, 2025 | DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;Class II · Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 | Device recalls |
| Jun 13, 2024 | Radiography 7300 CK233662 · KPR | 510(k) clearances |
| Jun 13, 2024 | Radiography 7300 CK233662 · Radiology | AI-enabled devices |
| Feb 14, 2024 | Radiography 7000 MK233678 · IZL | 510(k) clearances |
| Jan 11, 2024 | ProxiDiagnost N90 / Precision CRF (706110, 706400)K233945 · JAA | 510(k) clearances |
| Oct 19, 2023 | CombiDiagnost R90K232910 · JAA | 510(k) clearances |
| Dec 13, 2021 | Philips Radiology Smart AssistantK212186 · KPR | 510(k) clearances |
| Sep 21, 2021 | ProxiDiagnost N90K212837 · JAA | 510(k) clearances |
| May 19, 2021 | DigitalDiagnost 4 High Performance. radiography and fluoroscopy systemClass II · Following a system restart where the Table Height 2 (TH2) is the default setting and then switched to Wallstand VS2, ope | Device recalls |
| May 19, 2021 | ProxiDiagnost N90. radiography and fluoroscopy systemClass II · Following a system restart where the Table Height 2 (TH2) is the default setting and then switched to Wallstand VS2, ope | Device recalls |
| Apr 2, 2021 | DigitalDiagnostK210692 · KPR | 510(k) clearances |
| Dec 3, 2020 | CombiDiagnost R90K203087 · JAA | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
