Data / Medical devices / United States / Lira Center Inc
Lira Center Inc: FDA-registered device maker in Chicago, IL, United States, 1 510(k) clearance
Lira Center Inc is registered with the FDA (registration 3017144492) in Chicago, IL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 26, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017144492
- Address
- 730 N Franklin Street Suite 101, Chicago, IL, United States, 60654
- Owner or operator
- Lira Center Inc (10076071)
- Roles
- Repackager or relabeler
- First device listed
- December 1, 2022
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 2 | 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 |
|---|---|---|---|---|---|---|
| June 26, 2020 | K200736 | Stardust Med | GEX | Substantially Equivalent | I.T.S. Group S.R.L. | accessdata.fda.gov |
Compare with other makers
Updated June 26, 2020. 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.