Data / Medical devices / United States / Leeches U.S.A. Ltd.
Leeches U.S.A. Ltd.: FDA-registered device maker in Westbury, NY, United States, 1 510(k) clearance
Leeches U.S.A. Ltd. is registered with the FDA (registration 2419564) in Westbury, NY, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 21, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2419564
- FEI number
- 2434772
- Address
- 300 Shames DR., Westbury, NY, United States, 11590
- Owner or operator
- LEECHES U.S.A. LTD. (9003163)
- Roles
- Repackager or relabeler
- First device listed
- March 7, 2013
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Leeches, Medicinal | NRN | U | 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 21, 2004 | K040187 | MEDICINAL LEECHES | NRN | Substantially Equivalent | Ricarimpex Sas | accessdata.fda.gov |
Compare with other makers
Updated June 21, 2004. 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.