ZuriMED Technologies AG

ZuriMED Technologies AG holds 2 FDA 510(k) medical device clearances, first cleared 2024, most recent 2026.

Top product codes for ZuriMED Technologies AG

OWX — General, Plastic Surgery2 devices

Recent clearances by ZuriMED Technologies AG

K253867 — FiberLocker Implant; FiberLocker Instrument; FiberLocker PowerUnitCode OWX·2026-01-02
K241219 — FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instrument SN)Code OWX·2024-12-11

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