Data / Medical devices / China / Shanghai Seegen Photoelectric Technology Co., Ltd
Shanghai Seegen Photoelectric Technology Co., Ltd: FDA-registered device maker in Shanghai, China, 6 510(k) clearances
Shanghai Seegen Photoelectric Technology Co., Ltd is registered with the FDA (registration 3022106566) in Shanghai, China. It lists 7 device types. The FDA files 6 510(k) clearances under its listings, the newest dated January 30, 2026. Registered through 2026. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3022106566
- Address
- 3 Floor, Building No.1, 4299 JinDu Road Minhang District, Shanghai, China, 201108
- Owner or operator
- Shanghai SeeGen Photoelectric Technology Co., Ltd (10084506)
- Roles
- Manufacturer
- First device listed
- March 1, 2022
- Registered through
- 2026
- Brand names listed
- Disposable Distal End Tape Hood, Disposable Endoscope Valves Kit, Flexible Video-Choledo-Cysto-Ureteroscope System, Flexible Video-Choledochoscope, Flexible Video-Choledochoscope System, Imaging Processor System (Including Light Source)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Camera, Surgical And Accessories | KQM | 1 | Manufacturer | accessdata.fda.gov |
| Choledochoscope And Accessories, Flexible/Rigid | FBN | 2 | Manufacturer | accessdata.fda.gov |
| Colonoscope And Accessories, Flexible/Rigid | FDF | 2 | Manufacturer | accessdata.fda.gov |
| Endoscope Channel Accessory | ODC | 2 | Manufacturer | accessdata.fda.gov |
| Endoscopic Video Imaging System/Component, Gastroenterology-Urology | FET | 2 | Manufacturer | accessdata.fda.gov |
| Led Light Source | NTN | 2 | Manufacturer | accessdata.fda.gov |
| Ureteroscope And Accessories, Flexible/Rigid | FGB | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| January 30, 2026 | K252457 | Disposable Distal End Tape Hood | FDF | Substantially Equivalent | Shanghai SeeGen Photoelectric Technology Co., Ltd. | accessdata.fda.gov |
| March 7, 2025 | K243535 | Flexible Video-Choledochoscope (CHV-110J-U); Flexible Video-Choledochoscope (CHV-US120J-U) | FBN | Substantially Equivalent | Shanghai SeeGen Photoelectric Technology Co., Ltd. | accessdata.fda.gov |
| October 22, 2024 | K241532 | Flexible Video-Choledo-Cysto-Ureteroscope System (PL-2100) | FET | Substantially Equivalent | Shanghai SeeGen Photoelectric Technology Co., Ltd. | accessdata.fda.gov |
| November 22, 2023 | K222499 | Disposable Endoscope Valves Kit | ODC | Substantially Equivalent | Shanghai SeeGen Photoelectric Technology Co., Ltd. | accessdata.fda.gov |
| April 20, 2023 | K222261 | Flexible Video-Choledochoscope System | FBN | Substantially Equivalent | Shanghai SeeGen Photoelectric Technology Co., Ltd. | accessdata.fda.gov |
| February 22, 2022 | K211686 | Flexible Video-Choledo-Cysto-Ureteroscope System | FGB | Substantially Equivalent | Shanghai SeeGen Photoelectric Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Led Light Source
- All makers of Choledochoscope And Accessories, Flexible/Rigid
- All makers of Camera, Surgical And Accessories
- All makers of Endoscopic Video Imaging System/Component, Gastroenterology-Urology
- All makers of Ureteroscope And Accessories, Flexible/Rigid
- All makers of Colonoscope And Accessories, Flexible/Rigid
Updated January 30, 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.