Skip to content

Aso International Manila, Inc.

Philippines(FDA 510(k) applicant) Last updated 25 Oct 2026

Devices
1
Registries
FDA 510(k)FDA
FDA recalls
0

Catalogue1

  • AsoAligner Ref K201104

    Class II FDA 510(k) Active

What Aso International Manila, Inc. makes

Aso International Manila, Inc. manufactures the AsoAligner, a dental alignment system designed for orthodontic treatment to gradually reposition teeth without traditional braces.

The company’s portfolio is regulated under FDA Class II devices and includes submissions via the 510(k) pathway. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

How many devices does Aso International Manila, Inc. have in the registry?

The registry currently lists 1 device for Aso International Manila, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Aso International Manila, Inc.'s devices?

Among its 1 most recently registered device, Aso International Manila, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Aso International Manila, Inc.'s devices fall under?

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

What are the newest devices from Aso International Manila, Inc. in the registry?

The most recently registered devices listed for Aso International Manila, Inc. include AsoAligner.

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

Information

Address
Atlantica Building 5, Block 12, Phase 1, South Avenue, Cavite,Region IVa,
FDA FEI number
3014054179