Lambda S.p.A.
ItalyFDA applicant, unverified
- Devices
- 1
What Lambda S.p.A. makes
Lambda S.P.A. manufactures diode lasers designed for surgical use in medical procedures, including those performed by doctors. These devices are part of the Doctor Surgery Diode Lasers Family, intended for precision applications in clinical settings.
The company’s portfolio is regulated under FDA’s Class II device classification, with products listed via the 510(k) clearance pathway. Lambda S.P.A. is based in the United States.
Catalogue
Doctor Surgery Diode Lasers Family Ref K102036
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lambda S.P.A. have in the registry?
The registry currently lists 1 device for Lambda S.P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lambda S.P.A.'s devices?
Among its 1 most recently registered device, Lambda S.P.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Lambda S.P.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lambda S.P.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lambda S.P.A. in the registry?
The most recently registered devices listed for Lambda S.P.A. include DOCTOR SURGERY DIODE LASERS FAMILY.