Data / Medical devices / United States / Choytong LLC
Choytong LLC: FDA-registered device maker in Buffalo, NY, United States, 1 510(k) clearance
Choytong LLC is registered with the FDA (registration 3045019904) in Buffalo, NY, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 11, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3045019904
- Address
- 50 Fountain Plaza Suite 1400, Buffalo, NY, United States, 14202
- Owner or operator
- CHOYTONG LLC (10094395)
- Roles
- Repackager or relabeler
- First device listed
- December 23, 2025
- Registered through
- 2026
- Brand names listed
- Transducer Probe Cover
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Transducer, Ultrasonic, Diagnostic | ITX | 2 | Repackager or relabeler | 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 11, 2023 | K221278 | Transducer Probe Cover | ITX | Substantially Equivalent | Hony Medical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated January 11, 2023. 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.