Skip to content

Diemolding Corp.

United StatesFDA applicant, unverified

Devices
12

Catalogue12

Newest first, rows 1-12 of 12

Search and filter all 12 devices
Skip device list

Rows 1-12 of 12

Frequently asked questions

How many devices does Diemolding Corp. have in the registry?

The registry currently lists 12 devices for Diemolding Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Diemolding Corp.'s devices?

Among its 12 most recently registered devices, Diemolding Corp. has devices listed in FDA 510(k) (12 devices).

What risk classes do Diemolding Corp.'s devices fall under?

Among its 12 most recently registered devices, the classes recorded for Diemolding Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Diemolding Corp. in the registry?

The most recently registered devices listed for Diemolding Corp. include VACON TM, CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR, MEDSHIELD/AEROCHAMBER and RESPIREX 2.

Generated automatically from registry data and not verified by a human reviewer.