Data / Medical devices / Lice Removal Kit Containing A Solution / United States
FDA-registered makers of Lice Removal Kit Containing A Solution in the United States: 6 establishments
6 establishments in the United States are registered with the FDA to make Lice Removal Kit Containing A Solution (product code PUN). 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
- Lice Removal Kit Containing A Solution
- Product code
- PUN
- Country
- United States
Makers of Lice Removal Kit Containing A Solution 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 | 0 | 0 | 0 | 0 | api.fda.gov | |
| Freezenit, Inc. | Marblehead, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Larada Sciences Inc. | Salt Lake City, UT, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SCP Marketing & Distribution, LLC | Greensboro, NC, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Weeks & Leo Inc. | Clive, IA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| William V. Macgill & Co. | Lombard, IL, United States | Specification developer | 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.