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Data / Medical devices / Electrosurgical Coagulation For Aesthetic

Electrosurgical Coagulation For Aesthetic (ONQ): 3 FDA-registered makers in 3 countries

3 establishments in 3 countries are registered with the FDA to make Electrosurgical Coagulation For Aesthetic (product code ONQ, Class 2, 21 CFR 878.4400). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 4 510(k) clearances under this code, the latest on December 17, 2021, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
ONQ
Device class
2
Regulation
878.4400
Medical specialty
General, Plastic Surgery

Makers by country

CountryMakers
Belgium1
United States1
South Korea1

Makers of Electrosurgical Coagulation For Aesthetic

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
Fcare Systems NVBerchem Antwerpen, BelgiumManufacturer3December 17, 2021000api.fda.gov
Noreaster Medical LLCLincoln, RI, United StatesManufacturer1May 8, 2012000api.fda.gov
Classys IncAnyang-si Gyeonggi, South KoreaManufacturer0000api.fda.gov

Updated December 17, 2021. 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.