Data / Medical devices / Brazil / Ac Equipamentos Medicos E Odontologicos Ltda
Ac Equipamentos Medicos E Odontologicos Ltda: FDA-registered device maker in Ribeirao Preto Sao Paulo, Brazil, 1 510(k) clearance
Ac Equipamentos Medicos E Odontologicos Ltda is registered with the FDA (registration 3021741513) in Ribeirao Preto Sao Paulo, Brazil. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 1, 1986. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3021741513
- Address
- Rua Antonio Fernandes Figueroa No. 1786 Parque Ind. Lagoinha, Ribeirao Preto Sao Paulo, Brazil, 14095-280
- Owner or operator
- AC Equipamentos Medicos e Odontologicos LTDA (10057902)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- June 11, 2018
- Registered through
- 2026
- Brand names listed
- 1402 2HP Delivery System, 1403 2 HP Rear Mounted Delivery System, 1407 2HP Rear Mounted delivery system, 1407 3HP Delivery Systems, 1407 3HP delivery system, 1408 3 HP Rear Mounted Delivery System, 14083 HP Rear Mounted Delivery System, 1607Post Mounted Cuspidor and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chair, Dental, With Operative Unit | KLC | 1 | Contract manufacturer | accessdata.fda.gov |
| Chair, Dental, Without Operative Unit | NRU | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Operative Dental | EIA | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 1, 1986 | K863021 | CM-II, CM-I WATER UNIT | EIA | Substantially Equivalent | Sds Dental, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Chair, Dental, With Operative Unit
- All makers of Unit, Operative Dental
- All makers of Chair, Dental, Without Operative Unit
Updated October 1, 1986. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.