(1) A dental laboratory registered under ORS 679.710 shall provide to a prescribing dentist who submits a work order to the dental laboratory:
(a) A material content disclosure for each dental prosthetic appliance or other artificial material or device in a manner that is easily entered into the patient record; and
(b) The point of origin of the manufacture of each dental prosthetic appliance or other artificial material or device ordered under the work order.
(2) If a dental prosthetic appliance or other artificial material or device ordered under the work order was partially or entirely manufactured by one or more third parties, the point of origin disclosure described in subsection (1) of this section must identify:
(a) The portion of the dental prosthetic appliance or other artificial material or device that was manufactured by the third party; and
(b) The city, state and country of each third party.