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Framewerk LLC

Country not established

Framewerk LLC is a medical device manufacturer, with 1 device listed in FDA GUDID (FDA Class II) as of 14 Nov 2026.

Devices
1

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • FDA GUDID 1
Device classes
  • FDA Class II 1
Identifiers
  • DUNS 080774091

Catalogue1

Newest first, rows 1-1 of 1

Company details

DUNS number
080774091

Frequently asked questions

How many devices does FRAMEWERK LLC have in the registry?

The registry currently lists 1 device for FRAMEWERK LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list FRAMEWERK LLC's devices?

Among its 1 most recently registered device, FRAMEWERK LLC has devices listed in FDA GUDID (1 device).

What risk classes do FRAMEWERK LLC's devices fall under?

Among its 1 most recently registered device, the classes recorded for FRAMEWERK LLC's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from FRAMEWERK LLC in the registry?

The most recently registered devices listed for FRAMEWERK LLC include HTG Life PL-029G.

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