Data / Medical devices / United States / Wmi Enterprises, LLC
Wmi Enterprises, LLC: FDA-registered device maker in Indianapolis, IN, United States, 2 510(k) clearances
Wmi Enterprises, LLC is registered with the FDA (registration 3027321925) in Indianapolis, IN, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated April 2, 2026. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3027321925
- Address
- 7750 Zionsville Rd Ste 700, Indianapolis, IN, United States, 46268
- Owner or operator
- WMI Enterprises, LLC (10092492)
- Roles
- Repackager or relabeler
- First device listed
- January 14, 2025
- Registered through
- 2027
- Brand names listed
- Recovery+ Go
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Massager, Powered Inflatable Tube | IRP | 2 | Repackager or relabeler | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | 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 |
|---|---|---|---|---|---|---|
| April 2, 2026 | K253076 | Cryopush Cold Compression Device (A02-P-001) | IRP | Substantially Equivalent | Chengdu Cryo-Push Medical Technology Co.,Ltd | accessdata.fda.gov |
| December 5, 2022 | K222669 | Cryopush Cold Compression Device | IRP | Substantially Equivalent | Chengdu Cryo-Push Medical Technology Co.,Ltd | accessdata.fda.gov |
Compare with other makers
Updated April 2, 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.