Data / Medical devices / Floss, Dental / United States
FDA-registered makers of Floss, Dental in the United States: 61 establishments
61 establishments in the United States are registered with the FDA to make Floss, Dental (product code JES). 5 have 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
- Floss, Dental
- Product code
- JES
- Country
- United States
Makers of Floss, Dental in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| New World Imports, Inc. | Nashville, TN, United States | Specification developer | 1 | December 12, 1996 | 0 | 0 | 0 | api.fda.gov |
| Procter & Gamble Co., Regulatory Affairs | Mason, OH, United States | Specification developer | 1 | January 28, 1993 | 0 | 0 | 0 | api.fda.gov |
| Sunstar Americas, Inc. | Schaumburg, IL, United States | Manufacturer, Repackager or relabeler, Specification developer | 1 | June 28, 1995 | 0 | 0 | 0 | api.fda.gov |
| The Belport Company, Inc DBA Gingi-Pak | Camarillo, CA, United States | Manufacturer | 1 | September 8, 1981 | 0 | 0 | 0 | api.fda.gov |
| Ultradent Products Inc. | South Jordan, UT, United States | Manufacturer | 1 | June 16, 1992 | 0 | 0 | 0 | api.fda.gov |
| Amden Corp. | Carson City, NV, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ashtel Studios, Inc. | Ontario, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Aspen Surgical Products, Inc. | Caledonia, MI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioseal | Placentia, CA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Brightworks Products Inc. | Elk Grove Village, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| BiometerPlus USA, Inc. | Fremont, CA, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carwild Corp. | New London, CT, United States | Contract manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Coast Enterprise | Miramar, FL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Convii Inc | Santa Clara, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cordica Medical, Inc. | Morristown, TN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Colgate-Palmolive Company | Piscataway, NJ, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Doc Brands, Inc. | Knoxville, TN, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DR. Tung's Products | Kaneohe, HI, United States | Specification developer | 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 | |
| Davids Health Sciences, Inc. | Menifee, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dedeco International, Inc. | Long Eddy, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DenTek Oral Care, Inc. | Tarrytown, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dexter-Russell, Inc | Sturbridge, MA, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Glenroe, LLC | Milwaukee, WI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hager Worldwide, Inc. | Hickory, NC, United States | Complaint file establishment, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Havpak, Inc. | Malvern, PA, United States | Contract manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hayden Products LLC | New York, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Havpak, Inc. | Malvern, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| IPB Inc | Ogden, UT, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jordco, Inc. | Hillsboro, OR, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lather Inc. | Pasadena, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Loops, L.L.C. | Ferndale, WA, United States | Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Luvline LLC | Los Angeles, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtech Products, Inc. | Tarrytown, NY, United States | Complaint file establishment, 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 | |
| Nvena LLC | New Richmond, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Onlycare Inc | Denver, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ortho Organizers, Inc. | Savannah, GA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orvance, LLC | Caledonia, MI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Outdoor Nation, LLC. | Jacksonville Beach, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pearlyfloss LLC. | New York, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Peri-Swab, LLC | Great Neck, NY, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Periscope Enterprises, Inc. | Los Altos, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Practicon, Inc. | Greenville, NC, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PUL & Co. | Las Vegas, NV, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Protego LLC | Mountlake Ter, WA, 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 | |
| Radius Corporation | Kutztown, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ranir LLC | Grand Rapids, MI, United States | Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ready Set Import | Beverly Hills, CA, 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 | |
| Shummi Us LLC | Elk Grove Village, IL, United States | Contract manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Single Use Dental, Inc | Los Angeles, CA, United States | Repackager or relabeler, Reprocessor | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solventum Us LLC | Eagan, MN, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smyles Above Innovations, Inc | Barrington, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solventum US LLC | San Antonio, TX, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Kind Lab Inc | Coconut Grove, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tess Oral Health LLC | Eau Claire, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ultra Distributors | Somerset, NJ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vanmax, Inc | San Francisco, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zebra | Argyle, TX, 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.