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Myerson LLC

United Statesfrom the FDA registration address FDA establishment FEI 3003928050

Devices
1
Registrations
FDA
FDA recalls
0

Catalogue1

Newest first, rows 1-1 of 1

  • Trusana™ Ref K230098

    Active Regimes: 510(k) Registry: 510(k) Class:II

Company details

FDA FEI number
3003928050
Address
5106 N RAVENSWOOD AVE, Chicago, IL, 60640

Frequently asked questions

How many devices does MYERSON LLC have in the registry?

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

Which registries list MYERSON LLC's devices?

Among its 1 most recently registered device, MYERSON LLC has devices listed in FDA 510(k) (1 device).

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

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

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

The most recently registered devices listed for MYERSON LLC include Trusana™.

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.