Synthon Hispania S.L.

Synthon Hispania S.L. holds 1 FDA 510(k) medical device clearance, cleared in 2024.

Top product codes for Synthon Hispania S.L.

KZH — General Hospital1 device

Recent clearances by Synthon Hispania S.L.

K243232 — GripMateCode KZH·2024-12-02

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