Medical Device Manufacturer · IT , Via Col Di Lana

Lumen S.R.L. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1994

Total

Cleared

Denied

Lumen S.R.L. has 1 FDA 510(k) cleared medical devices. Based in Via Col Di Lana, IT.

Historical record: 1 cleared submissions from 1994 to 1994. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Lumen S.R.L. Filter by specialty or product code using the sidebar.

Lumen S.R.L. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Lumen S.R.L.

1 devices

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