BioStable Science & Engineering, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does BioStable Science & Engineering, Inc. have in the registry?
The registry currently lists 2 devices for BioStable Science & Engineering, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list BioStable Science & Engineering, Inc.'s devices?
Among its 2 most recently registered devices, BioStable Science & Engineering, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do BioStable Science & Engineering, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for BioStable Science & Engineering, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from BioStable Science & Engineering, Inc. in the registry?
The most recently registered devices listed for BioStable Science & Engineering, Inc. include HAART 200 Aortic Annuloplasty Device 19mm, HAART 200 Aortic Annuloplasty Device 21mm, HAART 200 Aortic Annuloplasty Device 23mm, HAART 200 Aortic Annuloplasty Device 25mm and HAART 300 Aortic Annuloplasty Device 19mm, HAART 300 Aortic Annuloplasty Device 21mm, HAART 300 Aortic Annuloplasty Device 23mm, HAART 300 Aortic Annuloplasty Device 25mm.