Data / Medical devices / Lice Removal Kit Containing A Solution
Lice Removal Kit Containing A Solution (PUN): 13 FDA-registered makers in 7 countries
13 establishments in 7 countries are registered with the FDA to make Lice Removal Kit Containing A Solution (product code PUN, Class 1, 21 CFR 880.5960). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- PUN
- Device class
- 1
- Regulation
- 880.5960
- Medical specialty
- General Hospital
Makers by country
| Country | Makers |
|---|---|
| United States | 6 |
| Belgium | 2 |
| Czechia | 1 |
| Poland | 1 |
| Netherlands | 1 |
| Australia | 1 |
| United Kingdom | 1 |
Makers of Lice Removal Kit Containing A Solution
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| 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 | |
| Aveflor | Kopidlno Jicin, Czechia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cosmade Belgium BV | Heist-op-den-Berg Antwerpen, Belgium | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Freezenit, Inc. | Marblehead, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Icb Pharma Tomasz Swietoslawski Pawel Swietoslawski | JAWORZNO Slaskie, Poland | Contract manufacturer, Exporter to the US, Manufacturer | 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 | |
| Oystershellnv | Merelbeke-Melle Oost-Vlaanderen, Belgium | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pronova Laboratories BV | Muiden Noord-Holland, Netherlands | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SCP Marketing & Distribution, LLC | Greensboro, NC, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Si&d (aust) Pty Ltd | Norwest New South Wales, Australia | Complaint file establishment, 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 | |
| Wordsworth (uk) Limited | Middleton Manchester, United Kingdom | 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.