Data / Medical devices / System, Suction, Lipoplasty / United States
FDA-registered makers of System, Suction, Lipoplasty in the United States: 16 establishments
16 establishments in the United States are registered with the FDA to make System, Suction, Lipoplasty (product code MUU). 7 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- System, Suction, Lipoplasty
- Product code
- MUU
- Country
- United States
Makers of System, Suction, Lipoplasty in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Solta Medical, Inc. | Bothell, WA, United States | Remanufacturer, Repackager or relabeler, Specification developer | 3 | September 17, 2012 | 0 | 0 | 0 | api.fda.gov |
| MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx | Carlsbad, CA, United States | Manufacturer | 2 | March 16, 2022 | 0 | 0 | 0 | api.fda.gov |
| Ranfac Corp. | Avon, MA, United States | Contract manufacturer, Manufacturer | 2 | January 19, 2017 | 0 | 0 | 0 | api.fda.gov |
| Summit Medical LLC | Saint Paul, MN, United States | Manufacturer | 2 | December 4, 2009 | 0 | 2 | 0 | api.fda.gov |
| EmCyte Corporation | Fort Myers, FL, United States | Manufacturer | 1 | November 7, 2019 | 0 | 0 | 0 | api.fda.gov |
| Jointechlabs, Inc | Brandon, FL, United States | Manufacturer | 1 | November 18, 2019 | 0 | 0 | 0 | api.fda.gov |
| Syntr Health Technologies, Inc. | Irvine, CA, United States | Complaint file establishment, Specification developer | 1 | July 2, 2021 | 0 | 0 | 0 | api.fda.gov |
| Ipax, Inc. | Englewood, CO, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Isomedix Operations, Inc. | Temecula, CA, United States | Contract sterilizer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| JG Plastics, Group LLC | Costa Mesa, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microaire Surgical Instruments LLC | Charlottesville, VA, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| PRO-TECH Design & Mfg, Inc. | Arlington, TX, 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 | |
| The Metrix Company | Dubuque, IA, 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.