Data / Medical devices / Warmer, Irrigation Solution / United States
FDA-registered makers of Warmer, Irrigation Solution in the United States: 15 establishments
15 establishments in the United States are registered with the FDA to make Warmer, Irrigation Solution (product code LHC). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Warmer, Irrigation Solution
- Product code
- LHC
- Country
- United States
Makers of Warmer, Irrigation Solution in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Mac Medical | Millstadt, IL, United States | Contract manufacturer, Manufacturer, Remanufacturer | 1 | June 13, 2008 | 0 | 0 | 0 | api.fda.gov |
| Blickman Industries LLC | Lawrenceburg, TN, United States | Remanufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Currie Medical, Inc. | Franklin, TN, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Currie Medical, Inc. | Norfolk, VA, United States | Manufacturer, Remanufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Genadyne Biotechnologies, Inc. | Hicksville, NY, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Haywood Vocational Opportunities Inc. | Waynesville, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MFG One, LLC | Chantilly, VA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microtek Medical LLC | Eagan, MN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microtek Medical LLC | Northfield, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microtek Medical LLC | Alpharetta, GA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pedigo Products, Inc. | Vancouver, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rac Medical Solutions | Bruceton, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tryptech Services | Greensboro, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| WEG Surgical Solutions | Greensboro, NC, United States | Specification developer | 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.