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Data / Medical devices / Needle, Interosseous

Needle, Interosseous (MHC): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Needle, Interosseous (product code MHC, Class 2, 21 CFR 880.5570). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on November 10, 2022, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
MHC
Device class
2
Regulation
880.5570
Medical specialty
General Hospital
Implant
Yes

Makers by country

CountryMakers
United States2
Israel1

Makers of Needle, Interosseous

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
Bard Access Systems, Inc.Salt Lake City, UT, United StatesSpecification developer2November 10, 2022000api.fda.gov
BiomericsSalt Lake City, UT, United StatesContract manufacturer0000api.fda.gov
Waismed Ltd.Rosh Haayin Central, IsraelManufacturer0000api.fda.gov

Updated November 10, 2022. 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.