Pulsaderm LLC
United StatesFDA applicant, unverified
Pulsaderm LLC is a medical device manufacturer, with 14 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 14
Registry facts
- Registries
- FDA GUDID 11
- FDA 510(k) 3
- Device classes
- FDA Class II 14
- Identifiers
- DUNS 080429881
What Pulsaderm LLC makes
Pulsaderm LLC manufactures phototherapy devices for skin and hair treatments, including red/blue light units, infrared lamps, and laser-based systems for hair growth. Their portfolio also includes transcutaneous neuromuscular electrical stimulation (TENS) units for physical therapy, as well as LED masks and combs designed for acne clearing and facial rejuvenation.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and UDI databases.
Catalogue
Search and filter all 14 devicesCompany details
- DUNS number
- 080429881
Frequently asked questions
How many devices does PULSADERM LLC have in the registry?
The registry currently lists 14 devices for PULSADERM LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list PULSADERM LLC's devices?
Among its 14 most recently registered devices, PULSADERM LLC has devices listed in FDA 510(k) (3 devices) and FDA GUDID (11 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do PULSADERM LLC's devices fall under?
Among its 14 most recently registered devices, the classes recorded for PULSADERM LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PULSADERM LLC in the registry?
The most recently registered devices listed for PULSADERM LLC include Pulsaderm PD9700R, Hair Laser Helmet RB2040, A.C.E Red and Blue PD9500 and NutraStim Hair Laser Comb PD8021NS.