Sorenson Laboratories, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Sorenson Laboratories, Inc. makes
Sorenson Laboratories, Inc. manufactures surgical laser instruments, including the CO₂ Handi-Lase for precise tissue procedures, and accessories like the Safe Air Vari-Spot handpiece telescope and adaptor for endoscopic applications. The company also produces the PlumeMaster smoke evacuation system, designed to manage surgical plume during procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Handi-Lase CO2 Surgical Laser Instrument Ref K920597
510(k) 510(k)- 510(k) 510(k)
Plumemaster Smoke Evacuation System Ref K930434
510(k) 510(k)
Frequently asked questions
How many devices does Sorenson Laboratories, Inc. have in the registry?
The registry currently lists 3 devices for Sorenson Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sorenson Laboratories, Inc.'s devices?
Among its 3 most recently registered devices, Sorenson Laboratories, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Sorenson Laboratories, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Sorenson Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sorenson Laboratories, Inc. in the registry?
The most recently registered devices listed for Sorenson Laboratories, Inc. include HANDI-LASE CO2 SURGICAL LASER INSTRUMENT, SAFE AIR VARI-SPOT HANDPIECE TELESCOPE AND ADAPTOR and PLUMEMASTER SMOKE EVACUATION SYSTEM.