Data / Medical devices / Dispenser, Solid Medication / United States
FDA-registered makers of Dispenser, Solid Medication in the United States: 18 establishments
18 establishments in the United States are registered with the FDA to make Dispenser, Solid Medication (product code NXB). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Dispenser, Solid Medication
- Product code
- NXB
- Country
- United States
Makers of Dispenser, Solid Medication in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Adco Intl Plastics Corp. | Marietta, GA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Apothecary Products, LLC. | Burnsville, MN, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Apothecary Products LLC dba IMS | Siren, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cordica Medical, Inc. | Woodstock, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Evans Manufacturing | Garden Grove, CA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fabrication Ent., Inc. | Elmsford, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HERO HEALTH, Inc. | New York, NY, United States | Manufacturer, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Omcare Inc | Bloomington, MN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pharmadva, LLC | Rochester, NY, United States | Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PatchRx, Inc. | Wilmington, DE, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Perigon Health 360 LLC | Plymouth, MI, United States | Complaint file establishment, 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 | |
| Richardson Products, Inc. | Frankfort, IL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Scribe Opco, LLC Dba Koozie Group | Spring Hill, FL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sequon, LLC | Annapolis, MD, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tenovi Co | Portsmouth, NH, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| iPill Inc | Rowland Heights, CA, 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.