Data / Medical devices / United States / Midway Medical
Midway Medical: FDA-registered device maker in Bloomington, IL, United States, 1 510(k) clearance
Midway Medical is registered with the FDA (registration 3015536408) in Bloomington, IL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 22, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015536408
- Address
- 3004 Gill Street Building 100, Bloomington, IL, United States, 61704
- Owner or operator
- Midway Medical (10061377)
- Roles
- Specification developer
- First device listed
- October 15, 2019
- Registered through
- 2026
- Brand names listed
- Plexus Portable DVT Therapy System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Sleeve, Limb, Compressible | JOW | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| July 22, 2019 | K190975 | Plexus SCD110 Sequential Compression Device Sleeve | JOW | Substantially Equivalent | Midway Medical, LLC | accessdata.fda.gov |
Compare with other makers
Updated July 22, 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.