POLIDENT d.o.o. Industrija dentalnih proizvodov, Dental Products Industry
Slovenian industrial manufacturer and exporter
POLIDENT d.o.o. Industrija dentalnih proizvodov, Dental Products Industry is listed by Sloexport in the other manufacturing sector. Its directory profile describes operations including Polident is a producer of medical devices for dentistry. Since 1958 we at Polident have been doing our best to offer top quality dental products to help you offer your clients the best possible treatment and aesthetic solutions. For our 55th anniversary, we present the new line of anatomical teeth REF-LINE for the most.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Volčja Draga, Slovenia
- Website
- https://polident.si
- Categories
- Pharmaceutical Manufacturing, Medical & Healthcare Supplies, Dental Supplies & Equipment
- Markets
- Slovenia, Austria, Germany, Italy, Croatia
Listed in a source registry
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
- sanctions-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)