Lasetech, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3015730775
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3015730775
- Address
- 11 Princess Road, Lawrenceville, NJ, 08648
Frequently asked questions
How many devices does LASETECH, LLC have in the registry?
The registry currently lists 3 devices for LASETECH, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list LASETECH, LLC's devices?
Among its 3 most recently registered devices, LASETECH, LLC has devices listed in FDA GUDID (3 devices).
What risk classes do LASETECH, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for LASETECH, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LASETECH, LLC in the registry?
The most recently registered devices listed for LASETECH, LLC include EpiCare-Zenith 504-ZTH, EpiCare-Zenith 504-ZTHY and EpiCare-Zenith 504-ZTHA.