Data / Medical devices / Unit, Oral Irrigation / United States
FDA-registered makers of Unit, Oral Irrigation in the United States: 26 establishments
26 establishments in the United States are registered with the FDA to make Unit, Oral Irrigation (product code EFS). 1 has 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
- Unit, Oral Irrigation
- Product code
- EFS
- Country
- United States
Makers of Unit, Oral Irrigation in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Twin River Group | Trenton, NJ, United States | Manufacturer | 1 | April 21, 1981 | 0 | 0 | 0 | api.fda.gov |
| Air Force Labs, Inc. | Holland, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ashtel Studios, Inc. | Ontario, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Conair LLC. | Stamford, CT, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| CranioMandibular Rehab, Inc. | Wheat Ridge, CO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Discus Dental, LLC | Ontario, CA, United States | Contract manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dreame Technology Usa Inc | Newark, DE, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fresh Health, Inc. Dba Proclaim Health | Mountain View, CA, United States | Complaint file establishment, Manufacturer, Remanufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Global TV Concepts, Ltd. | Coconut Creek, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| H2ofloss.inc | Ozone Park, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Havenrock Inc | San Diego, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| In'tech Industries | Ramsey, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inter-Med, Inc. | Racine, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Moon Oral Care, LLC. | El Segundo, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neuralpulse Ltd. | Albany, NY, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ontel Products Corporation | Fairfield, NJ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oratec Corp. | Manassas, VA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Panasonic Corporation Of North America | Newark, NJ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Parnell Pharmaceuticals, Inc. | San Rafael, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips Oral Healthcare, LLC | Bothell, WA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Poma Lifestyle Inc | Newark, DE, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quip Nyc Inc. | Brooklyn, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rosemarie Products Company, LLC | Mason, OH, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solite Wellbeing Usa Inc. | Austin, TX, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| TAO Clean, LLC | Millcreek, UT, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Water Pik, Inc. | Fort Collins, CO, United States | Complaint file establishment, 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.