Anadias, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Anadias, Inc. makes
Anadias, Inc. manufactures malar implants designed for facial reconstruction and nasal saw blades used in orthognathic or sinus surgery procedures.
The company’s portfolio includes Class I and Class II devices, all of which are listed under the FDA’s 510(k) pathway. These products are based in the United States.
Catalogue
Anadias Zara System Malar Implants Ref K871190
Regimes: 510(k) Registry: 510(k)Anadias Nasal Saw Blades Ref K854192
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anadias, Inc. have in the registry?
The registry currently lists 2 devices for Anadias, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anadias, Inc.'s devices?
Among its 2 most recently registered devices, Anadias, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Anadias, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Anadias, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anadias, Inc. in the registry?
The most recently registered devices listed for Anadias, Inc. include ANADIAS ZARA SYSTEM MALAR IMPLANTS and ANADIAS NASAL SAW BLADES.