Spiggle & Theis Medizintechnik GmbH - FDA 510(k) Cleared Devices
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) cleared devices by Spiggle & Theis Medizintechnik GmbH
1 devices