L.P. Systems Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What L.P. Systems Corp. makes
L.P. Systems Corp. manufactures the LPS 1118, a hair removal system designed for cosmetic use.
The company’s products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Lps 1118 Ref K820650
510(k) 510(k)Hair Removal System Ref K945192
510(k) 510(k)
Frequently asked questions
How many devices does L.P. Systems Corp. have in the registry?
The registry currently lists 2 devices for L.P. Systems Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list L.P. Systems Corp.'s devices?
Among its 2 most recently registered devices, L.P. Systems Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do L.P. Systems Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for L.P. Systems Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from L.P. Systems Corp. in the registry?
The most recently registered devices listed for L.P. Systems Corp. include LPS 1118 and HAIR REMOVAL SYSTEM.