Data / Medical devices / Nasal Spray, Ent Delivery / United States
FDA-registered makers of Nasal Spray, Ent Delivery in the United States: 17 establishments
17 establishments in the United States are registered with the FDA to make Nasal Spray, Ent Delivery (product code KCO). 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
- Nasal Spray, Ent Delivery
- Product code
- KCO
- Country
- United States
Makers of Nasal Spray, Ent Delivery in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Applied Laboratories, Inc. | Columbus, IN, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bayer Healthcare LLC, Consumer Care | Morristown, NJ, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Drmenta,inc | Albany, NY, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| FridaBaby LLC | Miami, FL, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GVK Corporation | Reno, NV, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hemostasis, LLC | Saint Paul, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| M&M Pure Air Systems LLC | Lewes, DE, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Merz Pharmaceuticals, LLC | Raleigh, NC, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mission Pharmacal Company | Boerne, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neilmed Pharmaceuticals, Inc. | Santa Rosa, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| North American Herb and Spice CO..LTD. LLC. | Mundelein, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rhinosystems, Inc. | Brooklyn, OH, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SMC Ltd. | Devens, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sheffield Pharmaceuticals LLC | New London, CT, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tesla Biohealing, Inc. | Milford, DE, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Mentholatum Company | Orchard Park, NY, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Unipack LLC | Pittsburgh, PA, United States | Contract manufacturer, 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.