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ABB Optical Group LLC.

Country not established FDA establishment FEI 2916547

Devices
1
Registrations
FDA
FDA recalls
0

Catalogue1

Newest first, rows 1-1 of 1

Company details

FDA FEI number
2916547
Address
3901 Ne 33rd Ter Ste E, Kansas City, MO, 64117

Frequently asked questions

How many devices does ABB Optical Group LLC. have in the registry?

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

Which registries list ABB Optical Group LLC.'s devices?

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

What risk classes do ABB Optical Group LLC.'s devices fall under?

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

What are the newest devices from ABB Optical Group LLC. in the registry?

The most recently registered devices listed for ABB Optical Group LLC. include BIOLENS Sphere (mangofilcon A) Soft (hydrophilic) Contact Lens for Daily Wear, BIOLENS Toric (mangofilcon A) Soft (hydrophilie) Contact Lens for Daily Wear, BIOLENS Multifocal (mangofilcon A) Soft (hydrophilic) contact lens for daily wear, BIOLENS Toric Multifocal (mangofilcon A) Soft (hydrophilic) contact lens for daily wear.

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.