Kavo do Brasil Indústria e Comércio de Equipamentos Odontológicos Ltda.
歯科用ハンドピース、ユニット、およびイメージング
KaVo Kerr のブラジル子会社で、高速歯科用ハンドピース、電気モーター、治療ユニットを製造しています。 KaVo do Brasil は、ラテンアメリカ全土の歯科医院や大学に供給しています。
- 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
- 医療およびヘルスケア用品, 歯科用品および歯科用機器
- Markets
- ブラジル, アルゼンチン, チリ, コロンビア
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)