W&H Dentalwerk Bürmoos GmbH

W&H Dentalwerk Bürmoos GmbH holds 2 FDA 510(k) medical device clearances, first cleared 2025, most recent 2026.

Top product codes for W&H Dentalwerk Bürmoos GmbH

DZI — Dental1 device
EFB — Dental1 device

Recent clearances by W&H Dentalwerk Bürmoos GmbH

K253655 — Angled Screwdriver MED (M-SD090)Code DZI·2026-07-31
K242179 — Synea Fusion Handpieces (Intensiv & Profin)Code EFB·2025-02-28

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