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
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Microaire Surgical Instruments LLC | Charlottesville, VA, United States | Manufacturer | 7 | April 25, 2025 | 0 | 0 | 0 | api.fda.gov |
| Black & Black Surgical, Inc. | Tucker, GA, United States | Manufacturer, Specification developer | 5 | September 13, 2024 | 0 | 0 | 0 | api.fda.gov |
| Solta Medical, Inc. | Bothell, WA, United States | Complaint file establishment, Manufacturer, Remanufacturer | 4 | May 1, 2019 | 0 | 0 | 0 | api.fda.gov |
| Apyx Medical Corporation | Clearwater, FL, United States | Manufacturer | 3 | August 21, 2026 | 0 | 0 | 0 | api.fda.gov |
| Mentor | Irving, TX, United States | Specification developer | 2 | July 1, 1998 | 0 | 0 | 0 | api.fda.gov |
| Arthrex, Inc. | Naples, FL, United States | Specification developer | 1 | July 30, 2014 | 0 | 0 | 0 | api.fda.gov |
| Bimini Health Tech | Plano, TX, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 1 | April 22, 2020 | 0 | 0 | 0 | api.fda.gov |
| HK Surgical, Inc. | San Clemente, CA, United States | Specification developer | 1 | November 19, 2003 | 0 | 0 | 0 | api.fda.gov |
| Kmi Imi Group / Dba: Innovative Med, Inc. | Irvine, CA, United States | Manufacturer | 1 | November 19, 2001 | 0 | 0 | 0 | api.fda.gov |
| Lipocosm, LLC | Key Biscayne, FL, United States | Specification developer | 1 | June 8, 2026 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Xomed, Inc. | Jacksonville, FL, United States | Manufacturer | 1 | January 21, 2000 | 0 | 0 | 0 | api.fda.gov |
| MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx | Carlsbad, CA, United States | Manufacturer | 1 | July 10, 2008 | 0 | 0 | 0 | api.fda.gov |
| Misonix, LLC | Farmingdale, NY, United States | Complaint file establishment, Manufacturer | 1 | May 17, 2004 | 0 | 0 | 0 | api.fda.gov |
| Pivot - Edm | La Vista, NE, United States | Contract manufacturer, Specification developer | 1 | December 30, 2024 | 0 | 0 | 0 | api.fda.gov |
| Tulip Medical Products, Inc. | San Diego, CA, United States | Manufacturer | 1 | April 27, 2006 | 0 | 0 | 0 | api.fda.gov |
| Armm, Inc. | Huntington Beach, CA, United States | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| B. Braun Us Device Manufacturing LLC | Allentown, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| P1 Technologies, Inc. | Cave Spring, VA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pivot International | Lenexa, KS, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Planet Innovation Products, Inc. | Irvine, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Primo Medical Group, INC | Stoughton, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Primo Medical Group, Inc | W Bridgewater, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Robling Medical, LLC | Youngsville, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Trident Manufacturing, Inc. | Pingree Grove, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.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.