Spiggle & Theis Medizintechnik GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Spiggle & Theis Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: TubaVent Balloon Dilatation System
1
Total
1
Cleared
0
Denied
Spiggle & Theis Medizintechnik GmbH has 1 FDA 510(k) cleared medical devices. Based in Overath, DE.
Last cleared in 2023. Active since 2023. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Spiggle & Theis Medizintechnik GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spiggle & Theis Medizintechnik GmbH
1 devices