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Synermed, Inc.

CanadaFDA 510(k) applicant, unverified

Devices
45

Catalogue45

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Frequently asked questions

How many devices does Synermed, Inc. have in the registry?

The registry currently lists 45 devices for Synermed, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Synermed, Inc.'s devices?

Among its 45 most recently registered devices, Synermed, Inc. has devices listed in FDA 510(k) (45 devices).

What risk classes do Synermed, Inc.'s devices fall under?

Among its 45 most recently registered devices, the classes recorded for Synermed, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Synermed, Inc. in the registry?

The most recently registered devices listed for Synermed, Inc. include AMP ALKALINE PHOSPHATASE REAGENT KIT, SYNERMED 600 NM URIC ACID REAGENT KIT, SYNERMED ISE REAGENTS and SYNERMED GGT REAGENT KIT.

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