Data / Medical devices / United States / Journey Medical Corporation
Journey Medical Corporation: FDA-registered device maker in Scottsdale, AZ, United States, 1 510(k) clearance
Journey Medical Corporation is registered with the FDA (registration 3012111117) in Scottsdale, AZ, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 1, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012111117
- Address
- 9237 E Via de Ventura Ste 105, Scottsdale, AZ, United States, 85258
- Owner or operator
- Journey Medical Corporation (10053691)
- Roles
- Manufacturer
- First device listed
- December 30, 2016
- Registered through
- 2026
- Brand names listed
- Luxamend
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Drug | FRO | U | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| May 1, 2013 | K122595 | HYDROPERMEATE TOPICAL EMULSION, ANSWER2SKIN SUNBURN RELIEF CREAM, ANSWER2SKIN FIRST AID CREAM | FRO | Substantially Equivalent | Dermal Life, LLC | accessdata.fda.gov |
Compare with other makers
Updated May 1, 2013. 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.