Apryse Software Corp.
United Statesfrom the FDA registration address FDA establishment FEI 3004915908
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
MiPACS V5 (1.0.0) Ref K260231
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3004915908
- Address
- 1927 S Tryon St Ste 200, CHARLOTTE, NC, 28203
Frequently asked questions
How many devices does Apryse Software Corp. have in the registry?
The registry currently lists 4 devices for Apryse Software Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Apryse Software Corp.'s devices?
Among its 4 most recently registered devices, Apryse Software Corp. has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Apryse Software Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Apryse Software Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Apryse Software Corp. in the registry?
The most recently registered devices listed for Apryse Software Corp. include MiPACS Dental Enterpise Viewer 4, MiPACS Storage Server 3, MiPACS HTML5 Web Viewer 3 and MiPACS V5 (1.0.0).