Data / Medical devices / China / Hangzhou Chohotech Co., Ltd
Hangzhou Chohotech Co., Ltd: FDA-registered device maker in Hangzhou Zhejiang, China, 1 510(k) clearance
Hangzhou Chohotech Co., Ltd is registered with the FDA (registration 3025359603) in Hangzhou Zhejiang, China. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 8, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3025359603
- Address
- room 405, building 5, lianchuang street 188, Yuhang District, Hangzhou Zhejiang, China, 311100
- Owner or operator
- Hangzhou ChohoTech Co., Ltd (10086116)
- Roles
- Manufacturer
- First device listed
- October 17, 2022
- Registered through
- 2026
- Brand names listed
- Intra oral camera (Ultra-S, Ultra-M, Ultra-L, Ultra-BP, Ultra-AP, Pro-S, Pro-M, Pro-L, Pro-BP, Pro-AP), LingOral Dental Design System, Retractor (iScan-AP);
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Retractor, Dental | EIF | 1 | Manufacturer | accessdata.fda.gov |
| Orthodontic Software | PNN | 2 | Manufacturer | accessdata.fda.gov |
| Retractor, All Types | EIG | 1 | Manufacturer | accessdata.fda.gov |
| System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations | NOF | 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 |
|---|---|---|---|---|---|---|
| May 8, 2026 | K260419 | LingOral Dental Design System | PNN | Substantially Equivalent | Hangzhou ChohoTech Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations
- All makers of Orthodontic Software
- All makers of Accessories, Retractor, Dental
- All makers of Retractor, All Types
Updated May 8, 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.