Data / Medical devices / Applicator, Vaginal / United States
FDA-registered makers of Applicator, Vaginal in the United States: 17 establishments
17 establishments in the United States are registered with the FDA to make Applicator, Vaginal (product code HGD). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Applicator, Vaginal
- Product code
- HGD
- Country
- United States
Makers of Applicator, Vaginal in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Apothecary Products, LLC. | Burnsville, MN, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Birchwood Laboratories LLC | Eden Prairie, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Casco Bay Molding | Sanford, ME, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cordica Medical, Inc. | Morristown, TN, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cordica Medical, Inc. | Woodstock, GA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cristcot LLC | Austin, TX, United States | Specification developer | 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 | |
| HTI Plastics, a Division of PCE Inc. | Lincoln, NE, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Huck Medical Technologies, Inc. (nichols) | Jacksonville, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mai/Genesis | Elmwood, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Organon LLC | Jersey City, NJ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pangaea Technologies LLC | The Woodlands, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pixie Cup LLC | Walnut Shade, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reia, LLC | Portland, ME, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SRC Medical, Inc. | Hanover, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SunMed Group Holdings, LLC | Grand Rapids, MI, United States | 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.