Data / Medical devices / Lavage, Jet / United States
FDA-registered makers of Lavage, Jet in the United States: 46 establishments
46 establishments in the United States are registered with the FDA to make Lavage, Jet (product code FQH). 9 have a 510(k) clearance or PMA approval on file and 5 have a recall event. FDA data exported November 2, 2026.
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- Device
- Lavage, Jet
- Product code
- FQH
- Country
- United States
Makers of Lavage, Jet in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Carefusion 2200, Inc. | Vernon Hills, IL, United States | Complaint file establishment, Specification developer | 3 | February 25, 2026 | 0 | 0 | 0 | api.fda.gov |
| Brasseler U.S.A. Medical, LLC | Savannah, GA, United States | Manufacturer | 2 | June 20, 1997 | 0 | 0 | 0 | api.fda.gov |
| Irrimax Corporation | Lawrenceville, GA, United States | Complaint file establishment, Specification developer | 2 | September 22, 2022 | 0 | 1 | 0 | api.fda.gov |
| Armis Biopharma, Inc. | Fort Collins, CO, United States | Complaint file establishment, Specification developer | 1 | May 25, 2023 | 0 | 0 | 0 | api.fda.gov |
| Enablecv, LLC | Midvale, UT, United States | Specification developer | 1 | January 29, 1993 | 0 | 0 | 0 | api.fda.gov |
| KDL Medical, Inc. | Richardson, TX, United States | Complaint file establishment, Manufacturer | 1 | January 6, 1998 | 0 | 0 | 0 | api.fda.gov |
| Kinamed, Inc. | Camarillo, CA, United States | Manufacturer | 1 | June 11, 1993 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Perfusion Systems | Minneapolis, MN, United States | Specification developer | 1 | December 8, 1997 | 0 | 1 | 0 | api.fda.gov |
| Medtronic Grand Rapids | Grand Rapids, MI, United States | Manufacturer | 1 | December 8, 1997 | 0 | 0 | 0 | api.fda.gov |
| American Spraytech, L.L.C. | Branchburg, NJ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Arobella Medical, LLC | Minnetonka, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Atrion Medical Products, Inc. | Arab, AL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Amsino Healthcare (USA) Inc. | Vernon Hills, IL, United States | Contract manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Boston Scientific Corporation | Marlborough, MA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biomerics Mebane | Mebane, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Boston Scientific Corporation | Coventry, RI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ClensTech Inc.dba ASEPT PAK INC. | Malone, NY, United States | Contract manufacturer, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Depuy Spine, Inc. | Raynham, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Deroyal Industries, Inc. | New Tazewell, TN, United States | Contract manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dvl-Op Medico Inc | Valencia, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Innovacyn, Inc. | Rialto, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| LivaNova USA, INC. | Arvada, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Med Michigan Holdings LLC | Lake Odessa, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microaire Surgical Instruments LLC | Charlottesville, VA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microport Orthopedics Inc. | Arlington, TN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Misonix, LLC | Farmingdale, NY, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Maquet Cardiovascular LLC | Wayne, NJ, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Medline Industries - Arlington Heights | Arlington Heights, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nortech Systems, Inc. | Milaca, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ontogen Manufacturing LLC | Lisle, IL, United States | Contract manufacturer | 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 | |
| Quality Tech Services, LLC | Bloomington, MN, 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 | |
| Rochal Technologies LLC | San Antonio, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smith & Nephew Inc. | Oklahoma City, OK, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smith & Nephew, Inc. | Memphis, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stiehl Tech | Lisle, IL, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Manufacturing Kalamazoo | Portage, MI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Puerto Rico, LLC. | Arroyo, PR, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smith & Nephew, Inc. | Memphis, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smith & Nephew, Inc. | Memphis, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Instruments | Portage, MI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Teleflex LLC (NADC) | Olive Branch, MS, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zimmer Manufacturing B.V. | Mercedita, PR, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zimmer Surgical, Inc. | Dover, OH, United States | Manufacturer, Specification developer | 0 | 0 | 1 | 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.