Data / Medical devices / Fentanyl And Other Opioid Protection Glove / United States
FDA-registered makers of Fentanyl And Other Opioid Protection Glove in the United States: 16 establishments
16 establishments in the United States are registered with the FDA to make Fentanyl And Other Opioid Protection Glove (product code QDO). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Fentanyl And Other Opioid Protection Glove
- Product code
- QDO
- Country
- United States
Makers of Fentanyl And Other Opioid Protection Glove in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| 4 Cascade Partners, LLC | Renton, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| American Armor Gloves | West Columbia, SC, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| American Nitrile Operations LLC | Grove City, OH, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Anrel Distribution LLC | Jackson, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ansell Healthcare Products LLC | Reno, NV, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bay Medical | Brisbane, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| D&M Procurement | Houston, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Genabio Diagnostics Inc | Bedford, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Labsource, Inc | Northlake, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Maxter Healthcare Inc | Rosharon, TX, United States | 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 | |
| North Coast Medical, Inc. | Morgan Hill, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| O&M Halyard, Inc. | Alpharetta, GA, United States | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sna Safehealth Solutions Inc. | Monrovia, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SW Technologies Inc. | Union City, CA, United States | Manufacturer, Remanufacturer, Repackager or relabeler, Reprocessor, Specification developer | 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.