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Data / Medical devices / System, Suction, Lipoplasty For Removal / United States

FDA-registered makers of System, Suction, Lipoplasty For Removal in the United States: 24 establishments

24 establishments in the United States are registered with the FDA to make System, Suction, Lipoplasty For Removal (product code QPB). 15 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
System, Suction, Lipoplasty For Removal
Product code
QPB
Country
United States

Makers of System, Suction, Lipoplasty For Removal in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Microaire Surgical Instruments LLCCharlottesville, VA, United StatesManufacturer7April 25, 2025000api.fda.gov
Black & Black Surgical, Inc.Tucker, GA, United StatesManufacturer, Specification developer5September 13, 2024000api.fda.gov
Solta Medical, Inc.Bothell, WA, United StatesComplaint file establishment, Manufacturer, Remanufacturer4May 1, 2019000api.fda.gov
Apyx Medical CorporationClearwater, FL, United StatesManufacturer3August 21, 2026000api.fda.gov
MentorIrving, TX, United StatesSpecification developer2July 1, 1998000api.fda.gov
Arthrex, Inc.Naples, FL, United StatesSpecification developer1July 30, 2014000api.fda.gov
Bimini Health TechPlano, TX, United StatesComplaint file establishment, Repackager or relabeler, Specification developer1April 22, 2020000api.fda.gov
HK Surgical, Inc.San Clemente, CA, United StatesSpecification developer1November 19, 2003000api.fda.gov
Kmi Imi Group / Dba: Innovative Med, Inc.Irvine, CA, United StatesManufacturer1November 19, 2001000api.fda.gov
Lipocosm, LLCKey Biscayne, FL, United StatesSpecification developer1June 8, 2026000api.fda.gov
Medtronic Xomed, Inc.Jacksonville, FL, United StatesManufacturer1January 21, 2000000api.fda.gov
MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA CellmyxCarlsbad, CA, United StatesManufacturer1July 10, 2008000api.fda.gov
Misonix, LLCFarmingdale, NY, United StatesComplaint file establishment, Manufacturer1May 17, 2004000api.fda.gov
Pivot - EdmLa Vista, NE, United StatesContract manufacturer, Specification developer1December 30, 2024000api.fda.gov
Tulip Medical Products, Inc.San Diego, CA, United StatesManufacturer1April 27, 2006000api.fda.gov
Armm, Inc.Huntington Beach, CA, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov
B. Braun Us Device Manufacturing LLCAllentown, PA, United StatesContract manufacturer0000api.fda.gov
P1 Technologies, Inc.Cave Spring, VA, United StatesContract manufacturer0000api.fda.gov
Pivot InternationalLenexa, KS, United StatesContract manufacturer0000api.fda.gov
Planet Innovation Products, Inc.Irvine, CA, United StatesContract manufacturer0000api.fda.gov
Primo Medical Group, INCStoughton, MA, United StatesContract manufacturer0000api.fda.gov
Primo Medical Group, IncW Bridgewater, MA, United StatesContract manufacturer0000api.fda.gov
Robling Medical, LLCYoungsville, NC, United StatesContract manufacturer0000api.fda.gov
Trident Manufacturing, Inc.Pingree Grove, IL, United StatesContract manufacturer0000api.fda.gov

Updated November 2, 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.