Spiggle & Theis Medizintechnik GmbH

1 FDA 510(k) medical device clearance.

Top product codes for Spiggle & Theis Medizintechnik GmbH

PNZ — Ear, Nose, Throat 1 device

Recent clearances by Spiggle & Theis Medizintechnik GmbH

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

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