Voco GmbH

Voco GmbH holds 119 FDA 510(k) medical device clearances, first cleared 1991, most recent 2026, with 4 FDA device recalls on record.

Clearances by Voco GmbH — page 2

101–119 of 119

K941124 — STRUCTUR 2Code EBG·1994-04-13
K930116 — LCL 8Code EMA·1993-06-17
K926492 — ARGION DENTAL CEMENTCode EMA·1993-04-08
K930455 — CHAMELEON LIGHT/CHEMICAL CURE GLASS IONOMERCode EMA·1993-04-08
K926418 — CLIPCode EBF·1993-03-31
K926419 — CALCICURCode EJK·1993-03-31
K926458 — BIFIX DENTAL CEMENTCode EMA·1993-03-31
K924181 — POLIBONDCode KLE·1992-10-16
K924182 — CALCIMOL LCCode EJK·1992-10-16
K923849 — CALCIMOLCode EJK·1992-09-28
K922853 — AQUA IONOFILCode EMA·1992-08-10
K922854 — AQUA MERONCode EMA·1992-08-05
K920365 — TOOTH BONDING AGENTCode EBF·1992-03-19
K915618 — PROVICOLCode EMA·1992-02-25
K915619 — IONOFIL/LONOFIL MOLARCode EMA·1992-02-25
K914612 — MERON DENTAL CEMENTCode EMA·1992-02-03
K914073 — F21(R) DENTAL CEMENTCode EMA·1991-10-21
K912495 — IONOSEALCode EJK·1991-07-30
K912497 — IONOBONDCode EMA·1991-07-30

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