Laurentian Laboratories
Country not established
- Devices
- 2
What Laurentian Laboratories makes
Laurentian Laboratories manufactures medical devices for securing intravenous lines and tubing, including the Universal Line-A-Plate and Universal Fix-A-Plate. These products are designed to stabilize and stabilize connections in intravenous administration sets, reducing disconnections during use.
The company’s portfolio is regulated as Class II devices under the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations. The manufacturer is based in the United States.
Catalogue
Universal Line-A-Plate Ref K833056
Regimes: 510(k) Registry: 510(k)Universal Fix-A-Plate Ref K833057
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laurentian Laboratories have in the registry?
The registry currently lists 2 devices for Laurentian Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laurentian Laboratories's devices?
Among its 2 most recently registered devices, Laurentian Laboratories has devices listed in FDA 510(k) (2 devices).
What risk classes do Laurentian Laboratories's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Laurentian Laboratories's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laurentian Laboratories in the registry?
The most recently registered devices listed for Laurentian Laboratories include UNIVERSAL LINE-A-PLATE and UNIVERSAL FIX-A-PLATE.