Data / Medical devices / United States / Dermalogica, LLC
Dermalogica, LLC: FDA-registered device maker in Carson, CA, United States, 1 510(k) clearance
Dermalogica, LLC is registered with the FDA (registration 1000561585) in Carson, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 25, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1000561585
- Address
- 1535 Beachey Pl, Carson, CA, United States, 90746
- Owner or operator
- Dermalogica, LLC (10094020)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- September 15, 2025
- Registered through
- 2027
- Brand names listed
- PRO Pen Microneedling System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Microneedle Device | QAI | 2 | Complaint file establishment, Specification developer | 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 |
|---|---|---|---|---|---|---|
| August 25, 2025 | K243800 | PRO Pen Microneedling System (6883) | QAI | Substantially Equivalent | Dermalogica, LLC | accessdata.fda.gov |
Compare with other makers
Updated August 25, 2025. 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.