Data / Medical devices / Adhesive, Denture, Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt / United States
FDA-registered makers of Adhesive, Denture, Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Adhesive, Denture, Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt (product code KOO). 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
- Adhesive, Denture, Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt
- Product code
- KOO
- Country
- United States
Makers of Adhesive, Denture, Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt 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 | November 30, 1994 | 0 | 0 | 0 | api.fda.gov |
| Andersonbrecon Inc. | Rockford, IL, United States | Contract manufacturer | 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 | |
| Procter & Gamble Co. | Brown Summit, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Procter & Gamble Co., Regulatory Affairs | Mason, OH, United States | 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 | |
| Sheffield Pharmaceuticals LLC | New London, CT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Uspharma Ltd | Miami Lakes, FL, United States | Manufacturer | 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.