Implacil DE Bortoli Material Odontologico Ltda
BrazilFDA applicant, unverified FDA FEI 3015775866
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Implacil DE Bortoli Material Odontologico Ltda makes
Implacil DE Bortoli Material Odontologico Ltda makes the Implacil Implant System, a dental implant system.
The Implacil Implant System is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Implacil Implant System Ref K202832
Regimes: 510(k) Registry: 510(k)Implacil Implant System Ref K183024
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3015775866
- Address
- RUA VICENTE DE CARVALHO, 178-182, Sao Paulo
Frequently asked questions
How many devices does Implacil DE Bortoli Material Odontologico Ltda have in the registry?
The registry currently lists 2 devices for Implacil DE Bortoli Material Odontologico Ltda. Devices recorded under merged duplicate company entries are counted once.
Which registries list Implacil DE Bortoli Material Odontologico Ltda's devices?
Among its 2 most recently registered devices, Implacil DE Bortoli Material Odontologico Ltda has devices listed in FDA 510(k) (2 devices).
What risk classes do Implacil DE Bortoli Material Odontologico Ltda's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Implacil DE Bortoli Material Odontologico Ltda's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Implacil DE Bortoli Material Odontologico Ltda in the registry?
The most recently registered devices listed for Implacil DE Bortoli Material Odontologico Ltda include Implacil Implant System.