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Spectrum Co.

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Spectrum Co. is a medical device manufacturer, with 107 devices listed in FDA GUDID and FDA 510(k) (FDA Class I, Class II and Unclassified) as of 13 Nov 2026.

Devices
107

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 104
  • FDA 510(k) 3

A device listed in two registries counts in both.

Device classes
  • FDA Class I 71
  • FDA Class II 22
  • FDA Unclassified 14

Catalogue107

Newest first, rows 1-50 of 107

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Rows 1-50 of 107

Showing 1-50 of 107

Frequently asked questions

How many devices does Spectrum Co. have in the registry?

The registry currently lists 107 devices for Spectrum Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Spectrum Co.'s devices?

Among its 50 most recently registered devices, Spectrum Co. has devices listed in FDA GUDID (50 devices).

What risk classes do Spectrum Co.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Spectrum Co.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Spectrum Co. in the registry?

The most recently registered devices listed for Spectrum Co. include Spectrum, Inc. 987-03897-000, Spectrum, Inc. 985-03502-000, Spectrum, Inc. 987-03605-000 and Spectrum, Inc. 982-03954-001.

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