Skip to content

Linde Gas & Equipment Inc.

United Statesfrom the FDA registration address FDA establishment FEI 2911183

Devices
17
Registrations
FDA
FDA recalls
0

Catalogue17

Newest first, rows 1-17 of 17

Search and filter all 17 devices
Skip device list

Rows 1-17 of 17

Company details

FDA FEI number
2911183
Address
1930 LOVERIDGE RD., Bay Point, CA, 94565

Frequently asked questions

How many devices does Linde Gas & Equipment Inc. have in the registry?

The registry currently lists 17 devices for Linde Gas & Equipment Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Linde Gas & Equipment Inc.'s devices?

Among its 17 most recently registered devices, Linde Gas & Equipment Inc. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (14 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Linde Gas & Equipment Inc.'s devices fall under?

Among its 17 most recently registered devices, the classes recorded for Linde Gas & Equipment Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Linde Gas & Equipment Inc. in the registry?

The most recently registered devices listed for Linde Gas & Equipment Inc. include NOxBOXi NOXKIT 2-15, NOxBOXi NOXKIT 1-10, MediPure Calibration Gas Mixtures 1 and NOxBOXi NOXKIT 2-22 1.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.