Lace Electronica S.r.l.
Country not established
- Devices
- 1
What Lace Electronica S.r.l. makes
Lace Electronica S.R.L. manufactures the GLAID Ocular Electrophysiology Device, a diagnostic tool used to assess retinal and optic nerve function through electrophysiological testing.
The device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Glaid Ocular Electrophysiology Device Ref K043367
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lace Electronica S.R.L. have in the registry?
The registry currently lists 1 device for Lace Electronica S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lace Electronica S.R.L.'s devices?
Among its 1 most recently registered device, Lace Electronica S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Lace Electronica S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lace Electronica S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lace Electronica S.R.L. in the registry?
The most recently registered devices listed for Lace Electronica S.R.L. include GLAID OCULAR ELECTROPHYSIOLOGY DEVICE.