Avalon Technology Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Avalon Technology Corp. makes
Avalon Technology Corp. manufactures medical imaging devices, including the AVALON GENERAL PURPOSE SCANNER, PREVIEW GP, a system for ultrasound imaging, and the ADMS MULTIPLANE RECTAL PROBE, designed for transrectal ultrasound examinations.
The company’s portfolio consists of Class II devices, authorised via the FDA’s 510(k) pathway, and is based in the United States.
Catalogue
Avalon General Purpose Scanner, Preview Gp Ref K904317
510(k) 510(k)Adms Multiplane Rectal Probe Ref K895359
510(k) 510(k)
Frequently asked questions
How many devices does Avalon Technology Corp. have in the registry?
The registry currently lists 2 devices for Avalon Technology Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avalon Technology Corp.'s devices?
Among its 2 most recently registered devices, Avalon Technology Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Avalon Technology Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Avalon Technology Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avalon Technology Corp. in the registry?
The most recently registered devices listed for Avalon Technology Corp. include AVALON GENERAL PURPOSE SCANNER, PREVIEW GP and ADMS MULTIPLANE RECTAL PROBE.