Data / Medical devices / Bronchoscope Accessory / China
FDA-registered makers of Bronchoscope Accessory in China: 5 establishments
5 establishments in China are registered with the FDA to make Bronchoscope Accessory (product code KTI). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Bronchoscope Accessory
- Product code
- KTI
- Country
- China
Makers of Bronchoscope Accessory in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alton Shanghai Medical Instruments Co Ltd | Shanghai, China | Complaint file establishment, Manufacturer | 1 | March 4, 2025 | 0 | 0 | 0 | api.fda.gov |
| Dongguan TT Medical, Inc. | Dongguan Guangdong, China | Manufacturer | 1 | March 1, 2023 | 0 | 0 | 0 | api.fda.gov |
| Micro-Tech (Nanjing) Co., Ltd. | Nanjing Jiangsu, China | Manufacturer | 1 | July 20, 2022 | 0 | 0 | 0 | api.fda.gov |
| Micro-Tech (Nanjing) Co., Ltd. | NAN JING Jiangsu, China | Manufacturer | 1 | July 20, 2022 | 0 | 0 | 0 | api.fda.gov |
| Smartdata Suzhou Co., Ltd | Suzhou Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.