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Data / Medical devices / Intra-Articular Orthopedic Stereotaxic Navigation Instrument

Intra-Articular Orthopedic Stereotaxic Navigation Instrument (SIQ): 3 FDA-registered makers in 1 country

3 establishments in 1 country are registered with the FDA to make Intra-Articular Orthopedic Stereotaxic Navigation Instrument (product code SIQ, Class 2, 21 CFR 888.4561). 3 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on July 6, 2026, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
SIQ
Device class
2
Regulation
888.4561
Medical specialty
Orthopedic

Makers by country

CountryMakers
United States3

Makers of Intra-Articular Orthopedic Stereotaxic Navigation Instrument

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
Smith & Nephew Inc.Oklahoma City, OK, United StatesManufacturer1July 6, 2026000api.fda.gov
Smith & Nephew Inc.Andover, MA, United StatesSpecification developer1July 6, 2026000api.fda.gov
Smith & Nephew Inc.Mansfield, MA, United StatesManufacturer1July 6, 2026000api.fda.gov

Updated July 6, 2026. 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.