Data / Medical devices / United States / Liberty Medical Solutions, LLC
Liberty Medical Solutions, LLC: FDA-registered device maker in Tampa, FL, United States, 1 510(k) clearance
Liberty Medical Solutions, LLC is registered with the FDA (registration 3012251759) in Tampa, FL, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 12, 2010. 1 recall event names it as the recalling firm. 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
- 3012251759
- Address
- 3653 Madaca Ln, Tampa, FL, United States, 33618
- Owner or operator
- Liberty Medical Solutions, LLC (10050855)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- January 12, 2016
- Registered through
- 2026
- Brand names listed
- Liberty Multi-Mode Stimulator
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Interferential Current Therapy | LIH | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Manufacturer, 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 |
|---|---|---|---|---|---|---|
| February 12, 2010 | K093138 | MT9000 SERIES ELECTRO-STIMULATOR, MODELS MT9000, MT9002, MT9001, MT9004 AND MT9003 | IPF | Substantially Equivalent | Shenzhen Dongdixin Technology Co., Ltd. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| November 3, 2023 | 93277 | Class II | Ongoing | Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation | The instruction manuals that were included with the Multi-Mode Stimulators distributed from 2018 to 2023 did not contain all of the appropriate warnings and contraindications. | accessdata.fda.gov |
Compare with other makers
- All makers of Interferential Current Therapy
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
- All makers of Stimulator, Muscle, Powered
Updated December 7, 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.