Cryptych Pty, Ltd.
AustraliaFDA 510(k) applicant, unverified
- Devices
- 7
What Cryptych Pty, Ltd. makes
Cryptych Pty, Ltd. manufactures the Nurochek System, a diagnostic device used for point-of-care testing, and Precision Screws, orthopedic fixation hardware designed for surgical applications.
The company’s products are regulated as Class II devices under the FDA’s 510(k) pathway. The Nurochek System and Precision Screws are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
Nurochek System Ref K200705
510(k) 510(k)Precision Screw Ref K160385
510(k) 510(k)
Company details
- DUNS number
- 742846228
Frequently asked questions
How many devices does Cryptych Pty, Ltd. have in the registry?
The registry currently lists 7 devices for Cryptych Pty, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cryptych Pty, Ltd.'s devices?
Among its 7 most recently registered devices, Cryptych Pty, Ltd. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Cryptych Pty, Ltd.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Cryptych Pty, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cryptych Pty, Ltd. in the registry?
The most recently registered devices listed for Cryptych Pty, Ltd. include Precision Screw CRY01-H3-1E, Precision Driver CRY02-H3, Precision Screw CRY01-H4-1E and Precision Tray CRY03.