Data / Medical devices / Lipoaspirate Washing System For Aesthetic Body Contouring / United States
FDA-registered makers of Lipoaspirate Washing System For Aesthetic Body Contouring in the United States: 15 establishments
15 establishments in the United States are registered with the FDA to make Lipoaspirate Washing System For Aesthetic Body Contouring (product code QKL). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Lipoaspirate Washing System For Aesthetic Body Contouring
- Product code
- QKL
- Country
- United States
Makers of Lipoaspirate Washing System For Aesthetic Body Contouring in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bimini Health Tech | Plano, TX, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Genesis Biosystems Inc. | Lewisville, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Globus Medical, Inc. | Audubon, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lifecell Corp | Branchburg, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lifecell Corp. | Branchburg, NJ, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Miami Fat Supply Inc | Fruitland Park, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Musculoskeletal Transplant Foundation d/b/a/ MTF Biologics | Olyphant, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Musculoskeletal Transplant Foundation d/b/a/ MTF Biologics | Edison, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Musculoskeletal Transplant Foundation d/b/a/ MTF Biologics | Jessup, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nessa Global Inc. | Dover, DE, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PRO-TECH Design & Mfg, Inc. | Arlington, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Summit Medical LLC | Saint Paul, MN, United States | Manufacturer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Synova Life Sciences, Inc. | Los Angeles, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Syntr Health Technologies, Inc. | Irvine, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tiger Aesthetics Medical-54 | Franklin, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.