Lase, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Lase, Inc. makes
Lase, Inc. manufactures medical devices for surgical smoke evacuation, including the ENVIROMATE™ Smoke Evacuation System, the LASE System II, and the LASE Evacuator/Aspirator. These products are designed to remove smoke, gases, and particulate matter generated during surgical procedures, improving operating room air quality and reducing exposure for staff and patients.
The company’s portfolio consists of Class II devices, each authorised through the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry, reflecting their regulatory compliance in the United States.
Catalogue
Enviromate(Tm) Smoke Evacuation System Ref K922555
Regimes: 510(k) Registry: 510(k)Lase System Ii Ref K871334
Regimes: 510(k) Registry: 510(k)Lase Evacuator/Aspirator Ref K874157
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lase, Inc. have in the registry?
The registry currently lists 3 devices for Lase, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lase, Inc.'s devices?
Among its 3 most recently registered devices, Lase, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Lase, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Lase, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lase, Inc. in the registry?
The most recently registered devices listed for Lase, Inc. include ENVIROMATE(TM) SMOKE EVACUATION SYSTEM, LASE SYSTEM II and LASE EVACUATOR/ASPIRATOR.