Data / Medical devices / Japan / Sony Corporation
Sony Corporation: FDA-registered device maker in Yokohama-shi Kanagawa, Japan, 10 510(k) clearances
Sony Corporation is registered with the FDA (registration 3004091527) in Yokohama-shi Kanagawa, Japan. It lists 9 device types. The FDA files 10 510(k) clearances under its listings, the newest dated August 26, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004091527
- Address
- 5-1-1, Minatomirai, Nishi-ku, Yokohama-shi Kanagawa, Japan, 220-8750
- Owner or operator
- Sony Corporation (9078461)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- November 28, 2006
- Registered through
- 2026
- Brand names listed
- HMS-3000MT SONY Monitor, HVO-3300MT SONY 3D HD VIDEO RECORDER, HVO-4000MT SONY 4K3D VIDEO RECORDERS, HVO-4000ST SONY 4K3D VIDEO RECORDERS, HVO-500MD SONY, HVO-550MD SONY, LMD-1530MD SONY Monitor, LMD-1951MD SONY Monitor and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Camera, Multi Format, Radiological | LMC | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Camera, Surgical And Accessories | KQM | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Device, Digital Image Storage, Radiological | LMB | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Endoscopic Video Imaging System/Component, Gastroenterology-Urology | FET | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Laparoscope, General & Plastic Surgery | GCJ | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Light, Surgical, Accessories | FTA | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| Microscope, Surgical | EPT | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| System, Digital Image Communications, Radiological | LMD | 1 | Complaint file establishment, Specification developer | accessdata.fda.gov |
| System, X-Ray, Tomography, Computed | JAK | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 26, 2026 | K260972 | OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD Monitor | GCJ | Substantially Equivalent | Sony Corporation | accessdata.fda.gov |
| January 10, 2020 | K191678 | IP Converter | GCJ | Substantially Equivalent | Sony Electronics, Inc. | accessdata.fda.gov |
| June 8, 2016 | K161122 | Sony IP Converter NU-IP40S | GCJ | Substantially Equivalent | Sony Electronics, Inc. | accessdata.fda.gov |
| July 29, 2015 | K150377 | Sony LMD-X310S LCD Monitor, Sony LMD-X310MD LCD Monitor, Sony LMD-X310NB LCD Monitor, Sony LMD-X550S LCD Monitor, Sony LMD-X550MD LCD, Sony LMD-X550NB LCD Monitor | GCJ | Substantially Equivalent | Sony Electronics, Inc. | accessdata.fda.gov |
| June 28, 2012 | K120611 | SONY PVM-2551MD OLED MONITOR | GCJ | Substantially Equivalent | Sony Electronics, Inc. | accessdata.fda.gov |
| February 24, 2012 | K113203 | SONY LMD-2451MT LCD MONITOR | GCJ | Substantially Equivalent | Sony Electronics, Inc. | accessdata.fda.gov |
| May 20, 1997 | K970999 | SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR | JAK | Substantially Equivalent | Sony Medical Systems | accessdata.fda.gov |
| July 3, 1996 | K961680 | SONY DKR-700 DIGITAL STILL RECORDER | LMB | Substantially Equivalent | Sony Medical Systems | accessdata.fda.gov |
| December 22, 1988 | K885042 | SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD | KQM | Substantially Equivalent | Sony Medical Electronics Co. | accessdata.fda.gov |
| August 4, 1988 | K882958 | SONY VIDEO PRINTERS, UP SERIES | KQM | Substantially Equivalent | Sony Medical Electronics Co. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Digital Image Communications, Radiological
- All makers of Laparoscope, General & Plastic Surgery
- All makers of Camera, Surgical And Accessories
- All makers of Device, Digital Image Storage, Radiological
- All makers of System, X-Ray, Tomography, Computed
- All makers of Light, Surgical, Accessories
Updated August 26, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.