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Data / Medical devices / Leeches, Medicinal

Leeches, Medicinal (NRN): 3 FDA-registered makers in 3 countries

3 establishments in 3 countries are registered with the FDA to make Leeches, Medicinal (product code NRN, Class U). 3 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 3 510(k) clearances under this code, the latest on August 7, 2015, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
NRN
Device class
U
Medical specialty
Unknown

Makers by country

CountryMakers
United Kingdom1
United States1
France1

Makers of Leeches, Medicinal

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Biopharm Uk LtdHENDY Carmarthenshire, United KingdomManufacturer1February 19, 2014000api.fda.gov
Carolina Biological Supply Co.Burlington, NC, United StatesManufacturer, Repackager or relabeler1August 7, 2015000api.fda.gov
RicarimpexEYSINES Nouvelle-Aquitaine, FranceManufacturer1June 21, 2004000api.fda.gov

Updated August 7, 2015. 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.