Kavo do Brasil Indústria e Comércio de Equipamentos Odontológicos Ltda.
Handpiece gigi, unit, dan pencitraan
Anak perusahaan KaVo Kerr di Brasil, yang memproduksi handpiece gigi berkecepatan tinggi, motor listrik, dan unit perawatan. KaVo do Brasil memasok klinik gigi dan universitas di seluruh Amerika Latin.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Joinville, Brazil
- Founded
- 1909
- Website
- https://www.kavo.com.br
- Categories
- Perlengkapan Medis & Kesehatan, Perlengkapan & Peralatan Gigi
- Markets
- Brasil, Argentina, Cile, Kolombia
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
- sanctions-clear (green), checked 2026-08-14 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-14 Mail server of the company domain
- domain-registered (green), checked 2026-08-14 Domain registry record
- debarment-clear (green), checked 2026-08-14 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- FDA Registered FDA Establishment Registration
- Good Manufacturing Practice
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)