Light Tree Ventures Europe B.V.
NetherlandsFDA applicant, unverified FDA FEI 3017422691
- Devices
- 14
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 14 devicesCompany details
- FDA FEI number
- 3017422691
- Address
- Saturnusstraat 95, 'S-Gravenhage Zuid-Holland
- Website
- www.lighttreeventures.com
- facebook.com/lighttreeventures
- [email protected]
- Phone
- +17866471640
From the company website
Discover innovative light therapy and medical device solutions with Light Tree Technology. From product development to manufacturing, we help bring your ideas to life.
Frequently asked questions
How many devices does Light Tree Ventures Europe B.V. have in the registry?
The registry currently lists 14 devices for Light Tree Ventures Europe B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Light Tree Ventures Europe B.V.'s devices?
Among its 14 most recently registered devices, Light Tree Ventures Europe B.V. has devices listed in FDA 510(k) (13 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Light Tree Ventures Europe B.V.'s devices fall under?
Among its 14 most recently registered devices, the classes recorded for Light Tree Ventures Europe B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Light Tree Ventures Europe B.V. in the registry?
The most recently registered devices listed for Light Tree Ventures Europe B.V. include RENEW Pro Facewear Mask PR4001, myLEDmask 2 (MJ-144), CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) and LED Lip Perfector, model: ZC-05.