Data / Medical devices / United States / Amenichi Consulting, LLC
Amenichi Consulting, LLC: FDA-registered device maker in Chicago, IL, United States, 1 510(k) clearance
Amenichi Consulting, LLC is registered with the FDA (registration 3019716369) in Chicago, IL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 18, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3019716369
- Address
- 222 Merchandise Mart Plz Ste 228, Chicago, IL, United States, 60654
- Owner or operator
- Amenichi Consulting, LLC (10082235)
- Roles
- Complaint file establishment
- First device listed
- November 19, 2025
- Registered through
- 2026
- Brand names listed
- Peribeam
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene | DXZ | 2 | Complaint file establishment | 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 18, 2025 | K240775 | PeriBeam® Pericardial Membrane | DXZ | Substantially Equivalent | Tamabio | accessdata.fda.gov |
Compare with other makers
Updated April 18, 2025. 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.