Vivadent (Usa), Inc.
Vivadent (Usa), Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1986.
Top product codes for Vivadent (Usa), Inc.
Recent clearances by Vivadent (Usa), Inc.
- K863831 — VIVADENT FILPIN
- K823409 — HELIOSIT-ORTHODONTIC
- K813015 — HELIOSEAL
- K802679 — SILANIT
- K802681 — HELIOBOND
- K802682 — CONTACT SEAL
- K802683 — HELIOSIT
- K802684 — HELIOMAT
- K802680 — ISOPAST-DS
- K802685 — REOLIT
- K801227 — SILICAP
- K801228 — BONDALCAP (SILICO-PHOSPHATE)
- K801229 — BONDALCAP (CARBOXYLATE)
- K790874 — AMALCAP-NON-GAMMA-2
- K790438 — COLORANT
- K790439 — CONTACT RESIN
- K781787 — ISOPLAST
Data sourced from openFDA. This site is unofficial and independent of the FDA.