Sandstone Medical Technologies, LLC
United StatesFDA applicant, unverified
- Devices
- 11
What Sandstone Medical Technologies, LLC makes
The company manufactures laser and intense pulsed light (IPL) systems for dermatological and aesthetic treatments, including CO₂, Nd:YAG, Er:YAG, ruby, and diode laser platforms. These devices are designed for procedures such as skin resurfacing, hair removal, tattoo removal, and vascular lesion treatment. The portfolio includes standalone laser systems, hybrid IPL/laser combinations, and CO₂ laser systems with scanning handpieces for precision applications.
All listed devices fall under Class II regulatory classification in the US and are authorised via 510(k) clearance through the FDA. The company’s products are registered under the US regulatory framework, with no mention of international listings or additional jurisdictions.
Catalogue
Search and filter all 11 devicesFrequently asked questions
How many devices does Sandstone Medical Technologies, LLC have in the registry?
The registry currently lists 11 devices for Sandstone Medical Technologies, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sandstone Medical Technologies, LLC's devices?
Among its 11 most recently registered devices, Sandstone Medical Technologies, LLC has devices listed in FDA 510(k) (11 devices).
What risk classes do Sandstone Medical Technologies, LLC's devices fall under?
Among its 11 most recently registered devices, the classes recorded for Sandstone Medical Technologies, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sandstone Medical Technologies, LLC in the registry?
The most recently registered devices listed for Sandstone Medical Technologies, LLC include APOLLO MINI IPL SYSTEM, LS-40 CO2 LASER SYSTEM MODEL LS-40, POLARIS Q-SWITCH RUBY SYSTEM and CHEVEUX DIODE LASER SYSTEM.