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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

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Twin River GroupTrenton, NJ, United StatesManufacturer1April 21, 1981000api.fda.gov
Air Force Labs, Inc.Holland, MI, United StatesManufacturer0000api.fda.gov
Ashtel Studios, Inc.Ontario, CA, United StatesSpecification developer0000api.fda.gov
Conair LLC.Stamford, CT, United StatesComplaint file establishment, Specification developer0000api.fda.gov
CranioMandibular Rehab, Inc.Wheat Ridge, CO, United StatesSpecification developer0000api.fda.gov
Discus Dental, LLCOntario, CA, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
Dreame Technology Usa IncNewark, DE, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Fresh Health, Inc. Dba Proclaim HealthMountain View, CA, United StatesComplaint file establishment, Manufacturer, Remanufacturer, Specification developer0000api.fda.gov
Global TV Concepts, Ltd.Coconut Creek, FL, United StatesSpecification developer0000api.fda.gov
H2ofloss.incOzone Park, NY, United StatesSpecification developer0000api.fda.gov
Havenrock IncSan Diego, CA, United StatesSpecification developer0000api.fda.gov
In'tech IndustriesRamsey, MN, United StatesContract manufacturer0000api.fda.gov
Inter-Med, Inc.Racine, WI, United StatesSpecification developer0000api.fda.gov
Moon Oral Care, LLC.El Segundo, CA, United StatesSpecification developer0000api.fda.gov
Neuralpulse Ltd.Albany, NY, United StatesManufacturer for export0000api.fda.gov
Ontel Products CorporationFairfield, NJ, United StatesSpecification developer0000api.fda.gov
Oratec Corp.Manassas, VA, United StatesSpecification developer0000api.fda.gov
Panasonic Corporation Of North AmericaNewark, NJ, United StatesSpecification developer0000api.fda.gov
Parnell Pharmaceuticals, Inc.San Rafael, CA, United StatesSpecification developer0000api.fda.gov
Philips Oral Healthcare, LLCBothell, WA, United StatesSpecification developer0000api.fda.gov
Poma Lifestyle IncNewark, DE, United StatesSpecification developer0000api.fda.gov
Quip Nyc Inc.Brooklyn, NY, United StatesSpecification developer0000api.fda.gov
Rosemarie Products Company, LLCMason, OH, United StatesSpecification developer0000api.fda.gov
Solite Wellbeing Usa Inc.Austin, TX, United StatesManufacturer, Specification developer0000api.fda.gov
TAO Clean, LLCMillcreek, UT, United StatesSpecification developer0000api.fda.gov
Water Pik, Inc.Fort Collins, CO, United StatesComplaint file establishment, Specification developer0000api.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.