Spiggle & Theis Medizintechnik GmbH

Spiggle & Theis Medizintechnik GmbH holds 1 FDA 510(k) medical device clearance, cleared in 2023.

Top product codes for Spiggle & Theis Medizintechnik GmbH

PNZ — Ear, Nose, Throat1 device

Recent clearances by Spiggle & Theis Medizintechnik GmbH

K223542 — TubaVent Balloon Dilatation SystemCode PNZ·2023-08-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.