Dermalogica, LLC
United Statesfrom the FDA registration address FDA FEI 1000561585
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Dermalogica, LLC makes
Dermalogica, LLC manufactures the PRO Pen Microneedling System, a handheld device designed for controlled microneedling treatments to improve skin texture and promote collagen production.
The PRO Pen Microneedling System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
PRO Pen Microneedling System (6883) Ref K243800
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000561585
- DUNS number
- 177698560
- Address
- 1535 Beachey Pl, Carson, CA, 90746
- [email protected]
- Phone
- +1 (800) 345-2761
Frequently asked questions
How many devices does Dermalogica, LLC have in the registry?
The registry currently lists 3 devices for Dermalogica, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermalogica, LLC's devices?
Among its 3 most recently registered devices, Dermalogica, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Dermalogica, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Dermalogica, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dermalogica, LLC in the registry?
The most recently registered devices listed for Dermalogica, LLC include PRO Pen Microneedling System 6883, PRO Pen 14-Pin Microneedling Cartridge 6819 and PRO Pen Microneedling System (6883).