Data / Medical devices / United States / The Kahen Group
The Kahen Group: FDA-registered device maker in Huntington Park, CA, United States, 1 510(k) clearance
The Kahen Group is registered with the FDA (registration 3042370478) in Huntington Park, CA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 23, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3042370478
- Address
- 2770 East Slauson Ave. Suite # East Slauson Ave. Suite #101, Huntington Park, CA, United States, 90255
- Owner or operator
- The Kahen Group (10094342)
- Roles
- Repackager or relabeler
- First device listed
- November 24, 2025
- Registered through
- 2026
- Brand names listed
- Avail Hygiene Reimagined
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Tampon, Menstrual, Scented, Scented-Deodorized | HIL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Pad, Menstrual, Unscented | HHD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Tampon, Menstrual, Unscented | HEB | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 23, 2004 | K042773 | ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONS | HIL | Substantially Equivalent | Rostam , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Pad, Menstrual, Unscented
- All makers of Tampon, Menstrual, Scented, Scented-Deodorized
- All makers of Tampon, Menstrual, Unscented
Updated November 23, 2004. 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.