Lpc, Inc.
Country not established
- Devices
- 1
What Lpc, Inc. makes
Lpc, Inc. manufactures spring-loaded pneumoperitoneum needles, designed for creating insufflation pathways during minimally invasive surgical procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Needle, Pneumoperitoneum, Spring Loaded Ref K924931
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lpc, Inc. have in the registry?
The registry currently lists 1 device for Lpc, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lpc, Inc.'s devices?
Among its 1 most recently registered device, Lpc, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Lpc, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lpc, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lpc, Inc. in the registry?
The most recently registered devices listed for Lpc, Inc. include NEEDLE, PNEUMOPERITONEUM, SPRING LOADED.