Data / Medical devices / Utensil, Eating / United States
FDA-registered makers of Utensil, Eating in the United States: 17 establishments
17 establishments in the United States are registered with the FDA to make Utensil, Eating (product code ILC). 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
- Utensil, Eating
- Product code
- ILC
- Country
- United States
Makers of Utensil, Eating in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| All Quality & Services, Inc. | Fremont, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ARK Products, LLC | Columbia, SC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ASP Global, LLC | Austell, GA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Altimate Medical, Inc. | Frankfort, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Avanos Medical, Inc. | Alpharetta, GA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bionix, LLC | Maumee, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Extreme Molding, LLC | Menands, NY, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ifd LLC | Jacksonville, FL, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Klann, Inc. | Waynesboro, VA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Myrava, LLC | Indianapolis, IN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| North Coast Medical, Inc. | Morgan Hill, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Performance Health Supply, LLC. | Cedarburg, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ProvaMed Inc | Birmingham, AL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reachable Technology | Cambridge, MA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Richardson Products, Inc. | Frankfort, IL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wilsons nc Enterprice LLC | Washington, NC, United States | Contract manufacturer, Manufacturer, Remanufacturer | 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.