Mano and Mano Proprietary Limited
AustraliaFDA applicant, unverified
- Devices
- 1
What Mano and Mano Proprietary Limited makes
Mano and Mano Proprietary Limited manufactures personal lubricants designed for use in medical and intimate health applications, providing hydration and comfort during physical activity or intimate relations.
The company’s products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer operates from the United States.
Catalogue
Mano and Mano Personal Lubricant Ref K161585
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mano and Mano Proprietary Limited have in the registry?
The registry currently lists 1 device for Mano and Mano Proprietary Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mano and Mano Proprietary Limited's devices?
Among its 1 most recently registered device, Mano and Mano Proprietary Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Mano and Mano Proprietary Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mano and Mano Proprietary Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mano and Mano Proprietary Limited in the registry?
The most recently registered devices listed for Mano and Mano Proprietary Limited include Mano and Mano Personal Lubricant.