Medical Device Manufacturer · DE , Germany

Gernot Lindner, Lunor-Vertrieb - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1993

Total

Cleared

Denied

Gernot Lindner, Lunor-Vertrieb has 1 FDA 510(k) cleared medical devices. Based in Germany, DE.

Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Gernot Lindner, Lunor-Vertrieb Filter by specialty or product code using the sidebar.

Gernot Lindner, Lunor-Vertrieb is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Gernot Lindner, Lunor-Vertrieb

1 devices

1-1 of 1