Data / Medical devices / United States / Sonicmed Medical Technology Co., Ltd
Sonicmed Medical Technology Co., Ltd: FDA-registered device maker in Las Vegas, NV, United States, 1 510(k) clearance
Sonicmed Medical Technology Co., Ltd is registered with the FDA (registration 3024490294) in Las Vegas, NV, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 31, 2019. Registered through 2026. FDA data exported November 2, 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
- 3024490294
- Address
- 5940 S Rainbow Blvd Ste 400 # 30327, Las Vegas, NV, United States, 89118
- Owner or operator
- SONICMED MEDICAL TECHNOLOGY CO., LTD (10086013)
- Roles
- Manufacturer
- First device listed
- October 10, 2022
- Registered through
- 2026
- Brand names listed
- Ultrasonic Surgical System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Instrument, Surgical, Sonic And Accessory/Attachment | JDX | 2 | Manufacturer | accessdata.fda.gov |
| Instrument, Ultrasonic Surgical | LFL | U | 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 |
|---|---|---|---|---|---|---|
| October 31, 2019 | K190281 | Ultrasonic Surgical System | LFL | Substantially Equivalent | Medisonic Technology CO | accessdata.fda.gov |
Compare with other makers
- All makers of Instrument, Ultrasonic Surgical
- All makers of Instrument, Surgical, Sonic And Accessory/Attachment
Updated October 31, 2019. 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.