Johnson & Johnson Produtos Profissionais Ltda.
Country not established
- Devices
- 1
What Johnson & Johnson Produtos Profissionais Ltda. makes
Johnson & Johnson Produtos Profissionais Ltda. manufactures the ORTHO ALL-FLEX DIAPHRAGM, a cervical diaphragm designed for contraceptive use.
The company’s products are regulated under FDA 510(k) clearance as Class II devices and are listed in the FDA’s 510(k) database. The manufacturer is based in the US.
Catalogue
Ortho All-Flex Diaphragm Ref K080040
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Johnson & Johnson Produtos Profissionais Ltda. have in the registry?
The registry currently lists 1 device for Johnson & Johnson Produtos Profissionais Ltda.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Johnson & Johnson Produtos Profissionais Ltda.'s devices?
Among its 1 most recently registered device, Johnson & Johnson Produtos Profissionais Ltda. has devices listed in FDA 510(k) (1 device).
What risk classes do Johnson & Johnson Produtos Profissionais Ltda.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Johnson & Johnson Produtos Profissionais Ltda.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Johnson & Johnson Produtos Profissionais Ltda. in the registry?
The most recently registered devices listed for Johnson & Johnson Produtos Profissionais Ltda. include ORTHO ALL-FLEX DIAPHRAGM.