Sheaumann Laser, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Sheaumann Laser, Inc. makes
Sheaumann Laser, Inc. manufactures laser systems, including the PL-1064 Laser System and the NeoLas, which are designed for medical applications requiring precise laser technology.
These devices fall under FDA Class II regulation and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
The Pl-1064 Laser System Ref K120938
Regimes: 510(k) Registry: 510(k)NeoLas Ref K150664
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sheaumann Laser, Inc. have in the registry?
The registry currently lists 2 devices for Sheaumann Laser, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sheaumann Laser, Inc.'s devices?
Among its 2 most recently registered devices, Sheaumann Laser, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Sheaumann Laser, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sheaumann Laser, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sheaumann Laser, Inc. in the registry?
The most recently registered devices listed for Sheaumann Laser, Inc. include THE PL-1064 LASER SYSTEM and NeoLas.