L & T S.N.C. DI E. Lucini & C.
ItalyFDA applicant, unverified
- Devices
- 1
What L & T S.N.C. DI E. Lucini & C. makes
L & T S.N.C. di E. Lucini & C. manufactures the LAPARO-TENSER, a device designed for laparoscopic surgical procedures, likely used to secure or stabilize tissues during minimally invasive operations.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the U.S. regulatory system. The manufacturer is based in the United States.
Catalogue
Laparo-Tenser Ref K970712
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does L & T S.N.C. DI E. Lucini & C. have in the registry?
The registry currently lists 1 device for L & T S.N.C. DI E. Lucini & C.. Devices recorded under merged duplicate company entries are counted once.
Which registries list L & T S.N.C. DI E. Lucini & C.'s devices?
Among its 1 most recently registered device, L & T S.N.C. DI E. Lucini & C. has devices listed in FDA 510(k) (1 device).
What risk classes do L & T S.N.C. DI E. Lucini & C.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for L & T S.N.C. DI E. Lucini & C.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from L & T S.N.C. DI E. Lucini & C. in the registry?
The most recently registered devices listed for L & T S.N.C. DI E. Lucini & C. include LAPARO-TENSER.