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Data / Medical devices / Diagnostic Ultrasonic Transducer, Robotic

Diagnostic Ultrasonic Transducer, Robotic (OQQ): 3 FDA-registered makers in 3 countries

3 establishments in 3 countries are registered with the FDA to make Diagnostic Ultrasonic Transducer, Robotic (product code OQQ, Class 2, 21 CFR 892.1570). 1 of them has 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 May 13, 2010, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
OQQ
Device class
2
Regulation
892.1570
Medical specialty
Radiology

Makers by country

CountryMakers
China1
United States1
Israel1

Makers of Diagnostic Ultrasonic Transducer, Robotic

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
Shenzhen Delica Medical Equipment Co., Ltd.SHENZHEN Guangdong, ChinaManufacturer1May 13, 2010000api.fda.gov
NeuraSignal, Inc.Los Angeles, CA, United StatesManufacturer0000api.fda.gov
Viasonix Ltd.RAANANA Central, IsraelManufacturer0000api.fda.gov

Updated May 13, 2010. 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.