L.A.S.E.R., Inc.
Country not established
- Devices
- 14
What L.A.S.E.R., Inc. makes
L.A.S.E.R., Inc. manufactures surgical instruments and laparoscopic devices, including disposable and reusable components for minimally invasive procedures. Their portfolio includes abdominal pressure control valves, grasping forceps, punches, and scissors, as well as alloy scalpel handpieces and trocar sleeves. They also produce insufflation tubing, bulk tissue removal systems, CO₂ laser models, endoscopic retractors, and titanium probes for surgical applications.
The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory submissions supported via the 510(k) pathway. Their products are listed in the FDA’s 510(k) database, reflecting compliance with U.S. medical device regulations. The manufacturer operates from the United States.
Catalogue
Search and filter all 14 devicesFrequently asked questions
How many devices does L.A.S.E.R., Inc. have in the registry?
The registry currently lists 14 devices for L.A.S.E.R., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list L.A.S.E.R., Inc.'s devices?
Among its 14 most recently registered devices, L.A.S.E.R., Inc. has devices listed in FDA 510(k) (14 devices).
What risk classes do L.A.S.E.R., Inc.'s devices fall under?
Among its 14 most recently registered devices, the classes recorded for L.A.S.E.R., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from L.A.S.E.R., Inc. in the registry?
The most recently registered devices listed for L.A.S.E.R., Inc. include ABDOMINAL PRESSURE CONTROL VALVE, GRASPING FORCEPS, PUNCHES, SCISSORS, ALLOY SCALPEL HANDPIECES and TROCAR SLEEVE.