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Data / Medical devices / Laser Assisted Lipolysis

Laser Assisted Lipolysis (ORK): 4 FDA-registered makers in 2 countries

4 establishments in 2 countries are registered with the FDA to make Laser Assisted Lipolysis (product code ORK, Class 2, 21 CFR 878.4810). 0 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 January 21, 2011, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
ORK
Device class
2
Regulation
878.4810
Medical specialty
General, Plastic Surgery

Makers by country

CountryMakers
China2
United States2

Makers of Laser Assisted Lipolysis

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
Beijing Perfectlaser Technology Co.,ltdBeijing, ChinaExporter to the US, Manufacturer0000api.fda.gov
Focus Medical, LLC.Bethel, CT, United StatesManufacturer, Specification developer0000api.fda.gov
Sanhe Jumei Technology Co.,ltdSanhe Hebei, ChinaExporter to the US, Manufacturer0000api.fda.gov
Sciton, Inc.Palo Alto, CA, United StatesComplaint file establishment, Manufacturer, Remanufacturer0000api.fda.gov

Updated January 21, 2011. 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.