Data / Medical devices / Pill Crusher/Cutter / United States
FDA-registered makers of Pill Crusher/Cutter in the United States: 17 establishments
17 establishments in the United States are registered with the FDA to make Pill Crusher/Cutter (product code OHY). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Pill Crusher/Cutter
- Product code
- OHY
- Country
- United States
Makers of Pill Crusher/Cutter in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alimed, LLC | Dedham, MA, United States | 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 | |
| ASP Global, LLC | Austell, GA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Assembly Required Di | Mount Sinai, NY, United States | Contract manufacturer | 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 | |
| Care Giver Supply LLC | Olivette, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ENOPREP, Inc | Big Canoe, GA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Evans Manufacturing | Garden Grove, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Health Care Logistics, Inc. | Circleville, OH, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hospi Corporation | San Mateo, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Minigrip Commercial LLC | Hauppauge, NY, United States | Contract 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 | |
| Ready Set Import | Beverly Hills, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Resolve Designs LLC | Springville, UT, United States | Manufacturer | 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 | |
| Velocity Concept Development Group, LLC | Cambridge, OH, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.