Data / Medical devices / Scraper, Tongue / United States
FDA-registered makers of Scraper, Tongue in the United States: 19 establishments
19 establishments in the United States are registered with the FDA to make Scraper, Tongue (product code LCN). 0 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
- Scraper, Tongue
- Product code
- LCN
- Country
- United States
Makers of Scraper, Tongue in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| 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 | |
| Contech Holdings LLC | Brea, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cordica Medical, Inc. | Morristown, TN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dale Medical Products, Inc. | New London, CT, United States | Manufacturer | 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 | |
| Davids Health Sciences, Inc. | Menifee, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DenTek Oral Care, Inc. | Tarrytown, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inter-Med, Inc. | Racine, WI, United States | Repackager or relabeler, 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 | |
| Mouthwatch, Inc. | Metuchen, NJ, 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 | |
| Profresh International Corp | Philadelphia, PA, 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 | Complaint file establishment, Repackager or relabeler, 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 | |
| Sunstar Americas, Inc. | Schaumburg, IL, United States | Repackager or relabeler, 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 |
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.